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Displasia cortical focal isolada tipo I
ORPHA:268961CID-10 · Q04.8CID-11 · LA05.51DOENÇA RARA
Esta doença tem causa genética. Recomendamos procurar um médico geneticista para diagnóstico, exames genéticos e aconselhamento familiar.
Também conhecida comoFCD
Sinônimos clínicos: FCD tipo I

Displasia cortical focal isolada tipo I é uma malformação cerebral congênita rara causada por mutações no gene SLC35A2. Caracteriza-se por uma área isolada de desenvolvimento cortical anormal, frequentemente associada a epilepsia de difícil controle.

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Introdução

O que você precisa saber de cara

Mantido pelo Disease Twin100% com fonte · atualizado 03/10/2026Revisão médica pendente
Informacoes curadas por IA — podem conter imprecisoes

Visão geral

A displasia cortical focal isolada tipo I (em inglês, Isolated focal cortical dysplasia type I) é uma condição rara identificada nos registros internacionais pelos códigos MONDO:0017095 e CID-10 Q04.8. Os dados epidemiológicos globais indicam que a sua prevalência exata é atualmente desconhecida.[1]

Causas genéticas

Estudos genéticos associam a condição a alterações no gene SLC35A2, o qual é responsável pela codificação da proteína transportadora de UDP-galactose (UDP-galactose translocator).[1][2]

Diagnóstico

Para a investigação diagnóstica e análise de bases moleculares, a literatura e as plataformas de dados genômicos registram a existência de 336 testes genéticos catalogados e 256 variantes relatadas no banco de dados ClinVar para avaliação.[1][2]

Fontes numeradas em Referências.

Conteúdo informativo gerado e mantido automaticamente a partir de fontes oficiais (Orphanet, HPO, OMIM, SUS). Não substitui avaliação médica.

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EM LINGUAGEM SIMPLES

A **displasia cortical focal isolada tipo I** (ou **FCD tipo I**) é uma alteração rara na formação do tecido cerebral, classificada formalmente pelo código Orpha 268961. Estudos genéticos relacionam esta condição a variantes no gene **SLC35A2**, havendo centenas de variações mapeadas na base internacional ClinVar. Na literatura médica, a condição é frequentemente investigada em cirurgias de controle de crises epilépticas focais na infância. No Brasil, a condição não possui um protocolo clínico próprio (PCDT) nem medicamentos específicos dispensados pelo SUS, sendo o suporte focado em procedimentos como exames genéticos e atendimento em reabilitação.

📋
Informacoes curadas por IA — podem conter imprecisoes

Displasia cortical focal isolada tipo I é uma malformação cerebral congênita rara causada por mutações no gene SLC35A2. Caracteriza-se por uma área isolada de desenvolvimento cortical anormal, frequentemente associada a epilepsia de difícil controle.

Publicações científicas
9 artigos
Último publicado: 2018 Jan

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
Unknown
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Worldwide
🏥
SUS: Cobertura mínimaScore: 15%
5 procedimentos SIGTAPCID-10: Q04.8
🇧🇷Dados SUS / DATASUS
EXAMES E PROCEDIMENTOS RELACIONADOS (5)
•
Cariótipo — bandas G, Q ou R
•
Pesquisa de microdeleções/microduplicações por FISH
•
Sequenciamento completo do exoma (WES)
•
Dosagem de alfa-fetoproteína
•
Atendimento em reabilitação — doenças raras
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

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Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa11
Total histórico9PubMed
Últimos 10 anos35publicações
Pico20155 papers
Linha do tempo
20202015Hoje · 2026
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

1 gene identificado com associação a esta condição.

SLC35A2UDP-galactose translocatorCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (1)
Transport of nucleotide sugars
MECANISMO DE DOENÇA

Congenital disorder of glycosylation 2M

An X-linked dominant, severe neurologic disorder characterized by developmental delay, hypotonia, ocular anomalies, and brain malformations. Othere more variable clinical features included seizures, hypsarrhythmia, poor feeding, microcephaly, recurrent infections, dysmorphic features, shortened limbs, and coagulation defects. Congenital disorders of glycosylation are caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins and a wide variety of clinical features. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.

EXPRESSÃO TECIDUAL(Ubíquo)
Fibroblastos
22.3 TPM
Pituitária
20.4 TPM
Esôfago - Mucosa
16.9 TPM
Pulmão
16.7 TPM
Glândula salivar
16.6 TPM
OUTRAS DOENÇAS (2)
SLC35A2-congenital disorder of glycosylationisolated focal cortical dysplasia type Ia
HGNC:11022UniProt:P78381

Variantes genéticas (ClinVar)

256 variantes patogênicas registradas no ClinVar.

🧬 SLC35A2: NM_005660.3(SLC35A2):c.1151C>T (p.Pro384Leu) ()
🧬 SLC35A2: NM_005660.3(SLC35A2):c.100C>A (p.Arg34Ser) ()
🧬 SLC35A2: NC_000023.11:g.48902933C>T ()
🧬 SLC35A2: NM_005660.3(SLC35A2):c.761A>G (p.Glu254Gly) ()
🧬 SLC35A2: NM_005660.3(SLC35A2):c.424C>T (p.Gln142Ter) ()
Ver todas no ClinVar

Classificação de variantes (ClinVar)

Distribuição de 1.406 variantes classificadas pelo ClinVar.

914
492
Patogênica (65.0%)
VUS (35.0%)
VARIANTES MAIS SIGNIFICATIVAS
TSC1: NM_000368.5(TSC1):c.631G>T (p.Glu211Ter) [Pathogenic]
TSC2: NM_000548.5(TSC2):c.4618_4619del (p.Tyr1540fs) [Pathogenic]
TSC2: NM_000548.5(TSC2):c.1445_1448del (p.Glu482fs) [Likely pathogenic]
TSC2: NC_000016.9:g.(?_2131598)_(2138613_?)del [Pathogenic]
MIR1225: NC_000016.9:g.(?_2120457)_(2185690_?)del [Pathogenic]

Vias biológicas (Reactome)

2 vias biológicas associadas aos genes desta condição.

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Displasia cortical focal isolada tipo I

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Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

Pesquisa e ensaios clínicos

Nenhum ensaio clínico registrado para esta condição.

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Publicações mais relevantes

Timeline de publicações
4 papers (10 anos)
#1

Isolated hippocampal sclerosis and focal dysplasia type IIIa: Comparative study of anatomo-electro-clinical profile and seizure outcome.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology2026 Jan

Distinguishing drug-resistant temporal lobe epilepsy (TLE) caused by isolated hippocampal sclerosis (iHS) from focal cortical dysplasia type IIIa (FCD IIIa) remains a presurgical challenge. This study aimed to compare the clinical characteristics, electrophysiological data, and postsurgical seizure outcomes between these pathologies. We retrospectively analyzed a cohort of 50 consecutive TLE patients (mean duration of disease of 22 years) who underwent surgery. The histopathology confirmed either iHS (n = 22) or FCD IIIa (n = 28) and a minimum follow-up of 12 months. The groups were compared on complex presurgical data, surgery type, and outcome. A history of febrile seizures (p = 0.02, OR = 4.7) was more frequent in the FCD IIIa group, which also had significantly lower intelligence quotient (IQ) scores in all domains. The mean total IQ score for FCD IIIa/iHS was 86/94 (p = 0.02); verbal IQ was 85/92 (p = 0.03); performance IQ was 89/98 (p = 0.02). The effect size was considered medium for all three (Cohen's d = 0.7, 0.63 and 0.68 respectively). Scalp EEG showed shorter seizures in FCD IIIa (p = 0.03), in SEEG, the temporal pole was more implanted in this group (p = 0.02, 50 % difference, OR = ∞). At a mean follow-up of 8.5 years, similar seizure-freedom rates was found between groups (82 % for FCD IIIa, 95 % for iHS; p = 0.48). Follow-up EEG and neuropsychological assessment at 6 months post-surgery showed no statistical differences. FCD IIIa and iHS exhibit several distinct electro-clinical features. The most important is a more impaired general cognitive profile associated with FCD IIIa, without differences in language or global memory.

#2

Identifying the epileptogenic zone by 18F-FDG PET/MRI in drug-resistant epilepsy with focal cortical dysplasia type IIIa.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology2026 Jan

Focal cortical dysplasia (FCD) type IIIa, distinct from isolated FCD in drug-resistant epilepsy, is typically confirmed via postoperative histopathology. This study aimed to evaluate the diagnostic utility of preoperative noninvasive 18F-fludeoxyglucose (FDG) PET/MRI co-registration in localizing the epileptogenic zone (EZ) in FCD type IIIa. We performed a retrospective study that included 60 patients with FCD type IIIa who underwent resection for drug-resistant epilepsy. The sensitivity of each modality for localizing the EZ was calculated, with invasive stereoelectroencephalography (SEEG) as a reference. Diagnostic accuracy and value of each modality were further assessed with respect to SEEG and postoperative outcomes for all patients and MRI negative/doubtful patients. We analyzed the diagnostic value of the different non-invasive diagnostic techniques with respect to concordance with SEEG findings and postsurgical seizure outcomes. For all included patients, 18F-FDG PET/MRI showed the highest sensitivity (75.7 %) for localizing the EZ across all modalities. We also found that 18F-FDG PET/MRI demonstrated the best accuracy and diagnostic value for localizing the EZ (60.0 %). Among MRI-doubtful/negative patients, 18F-FDG PET/MRI not only showed the highest sensitivity (79.3 %) but also achieved most promising accuracy and diagnostic value for identifying the EZ (61.7 % accuracy) across all modalities. 18F-FDG PET/MRI coregistration appears to be overwhelmingly rewarding in affording localization of EZ for patients with FCD type IIIa. This technique is potentially valuable as a noninvasive method to identify the EZ in patients with drug-resistant epilepsy due to FCD type IIIa, especially for MRI-negative/doubtful patients.

#3

A new perspective on drug-resistant epilepsy in children with focal cortical dysplasia type 1: From challenge to favorable outcome.

Epilepsia2025 Mar

We comprehensively characterized a large pediatric cohort with focal cortical dysplasia (FCD) type 1 to expand the phenotypic spectrum and to identify predictors of postsurgical outcomes. We included pediatric patients with histopathological diagnosis of isolated FCD type 1 and at least 1 year of postsurgical follow-up. We systematically reanalyzed clinical, electrophysiological, and radiological features. The results of this reanalysis served as independent variables for subsequent statistical analyses of outcome predictors. All children (N = 31) had drug-resistant epilepsy with varying impacts on neurodevelopment and cognition (presurgical intelligence quotient [IQ]/developmental quotient scores = 32-106). Low presurgical IQ was associated with abnormal slow background electroencephalographic (EEG) activity and disrupted sleep architecture. Scalp EEG showed predominantly multiregional and often bilateral epileptiform activity. Advanced epilepsy magnetic resonance imaging (MRI) protocols identified FCD-specific features in 74.2% of patients (23/31), 17 of whom were initially evaluated as MRI-negative. In six of eight MRI-negative cases, fluorodeoxyglucose-positron emission tomography (PET) and subtraction ictal single photon emission computed tomography coregistered to MRI helped localize the dysplastic cortex. Sixteen patients (51.6%) underwent invasive EEG. By the last follow-up (median = 5 years, interquartile range = 3.3-9 years), seizure freedom was achieved in 71% of patients (22/31), including seven of eight MRI-negative patients. Antiseizure medications were reduced in 21 patients, with complete withdrawal in six. Seizure outcome was predicted by a combination of the following descriptors: age at epilepsy onset, epilepsy duration, long-term invasive EEG, and specific MRI and PET findings. This study highlights the broad phenotypic spectrum of FCD type 1, which spans far beyond the narrow descriptions of previous studies. The applied multilayered presurgical approach helped localize the epileptogenic zone in many previously nonlesional cases, resulting in improved postsurgical seizure outcomes, which are more favorable than previously reported for FCD type 1 patients.

#4

Surgical outcomes in children with drug-resistant epilepsy and hippocampal sclerosis.

Epilepsy research2024 Jul

Hippocampal sclerosis (HS) is a common surgical substrate in adult epilepsy surgery cohorts but variably reported in various pediatric cohorts. We aimed to study the epilepsy phenotype, radiological and pathological variability, seizure and neurocognitive outcomes in children with drug-resistant epilepsy and hippocampal sclerosis (HS) with or without additional subtle signal changes in anterior temporal lobe who underwent surgery. This retrospective study enrolled children with drug-resistant focal epilepsy and hippocampal sclerosis with or without additional subtle T2-Fluid Attenuated Inversion Recovery (FLAR)/Proton Density (PD) signal changes in anterior temporal lobe who underwent anterior temporal lobectomy with amygdalohippocampectomy. Their clinical, EEG, neuropsychological, radiological and pathological data were reviewed and summarized. Thirty-six eligible patients were identified. The mean age at seizure onset was 3.7 years; 25% had daily seizures at time of surgery. Isolated HS was noted in 22 (61.1%) cases and additional subtle signal changes in ipsilateral temporal lobe in 14 (38.9%) cases. Compared to the normative population, the group mean performance in intellectual functioning and most auditory and visual memory tasks were significantly lower than the normative sample. The mean age at surgery was 12.3 years; 22 patients (61.1%) had left hemispheric surgeries. ILAE class 1 outcomes was seen in 28 (77.8%) patients after a mean follow up duration of 2.3 years. Hippocampal sclerosis was noted pathologically in 32 (88.9%) cases; type 2 (54.5%) was predominant subtype where further classification was possible. Additional pathological abnormalities were seen in 11 cases (30.6%); these had had similar rates of seizure freedom as compared to children with isolated hippocampal sclerosis/gliosis (63.6% vs 84%, p=0.21). Significant reliable changes were observed across auditory and visual memory tasks at an individual level post surgery. Favourable seizure outcomes were seen in most children with isolated radiological hippocampal sclerosis. Patients with additional pathological abnormalities had similar rates of seizure freedom as compared to children with isolated hippocampal sclerosis/gliosis.

#5

Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique.

Epilepsia2024 Jun

Recent studies have identified brain somatic variants as a cause of focal epilepsy. These studies relied on resected tissue from epilepsy surgery, which is not available in most patients. The use of trace tissue adherent to depth electrodes used for stereo electroencephalography (EEG) has been proposed as an alternative but is hampered by the low cell quality and contamination by nonbrain cells. Here, we use our improved depth electrode harvesting technique that purifies neuronal nuclei to achieve molecular diagnosis in a patient with focal cortical dysplasia (FCD). Depth electrode tips were collected, pooled by brain region and seizure onset zone, and nuclei were isolated and sorted using fluorescence-activated nuclei sorting (FANS). Somatic DNA was amplified from neuronal and astrocyte nuclei using primary template amplification followed by exome sequencing of neuronal DNA from the affected pool, unaffected pool, and saliva. The identified variant was validated using droplet digital polymerase chain reaction (PCR). An 11-year-old male with drug-resistant genetic-structural epilepsy due to left anterior insula FCD had seizures from age 3 years. Stereo EEG confirmed seizure onset in the left anterior insula. The two anterior insula electrodes were combined as the affected pool and three frontal electrodes as the unaffected pool. FANS isolated 140 neuronal nuclei from the affected and 245 neuronal nuclei from the unaffected pool. A novel somatic missense MTOR variant (p.Leu489Met, CADD score 23.7) was identified in the affected neuronal sample. Droplet digital PCR confirmed a mosaic gradient (variant allele frequency = .78% in affected neuronal sample; variant was absent in all other samples). Our findings confirm that harvesting neuronal DNA from depth electrodes followed by molecular analysis to identify brain somatic variants is feasible. Our novel method represents a significant improvement compared to the previous method by focusing the analysis on high-quality cells of the cell type of interest.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC3 artigos no totalmostrando 34

2026

Isolated hippocampal sclerosis and focal dysplasia type IIIa: Comparative study of anatomo-electro-clinical profile and seizure outcome.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
2026

Identifying the epileptogenic zone by 18F-FDG PET/MRI in drug-resistant epilepsy with focal cortical dysplasia type IIIa.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
2025

A new perspective on drug-resistant epilepsy in children with focal cortical dysplasia type 1: From challenge to favorable outcome.

Epilepsia
2024

Surgical outcomes in children with drug-resistant epilepsy and hippocampal sclerosis.

Epilepsy research
2024

Identification of a mosaic MTOR variant in purified neuronal DNA in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique.

Epilepsia
2023

The specific DNA methylation landscape in focal cortical dysplasia ILAE type 3D.

Acta neuropathologica communications
2023

The somatic p.T81dup variant in AKT3 gene underlies a mild cerebral phenotype and expands the spectrum including capillary malformation and lateralized overgrowth.

Genes, chromosomes &amp; cancer
2023

Ultra-Low Level Somatic Mutations and Structural Variations in Focal Cortical Dysplasia Type II.

Annals of neurology
2022

An Investigation into the Correlation of Scalp Electrophysiological Findings with Preoperative Clinical and Imaging Findings in Patients with Focal Cortical Dysplasia.

Turkish neurosurgery
2022

Focal cortical dysplasia: Updates.

Indian journal of pathology &amp; microbiology
2022

Significant Therapeutic Effects of Adult Human Neural Stem Cells for Spinal Cord Injury Are Mediated by Monocyte Chemoattractant Protein-1 (MCP-1).

International journal of molecular sciences
2022

A Novel De Novo TUBB3 Variant Causing Developmental Delay, Epilepsy and Mild Ophthalmological Symptoms in a Chinese Child.

Journal of molecular neuroscience : MN
2021

Cognitive and behavioral profiles of pediatric surgical candidates with frontal and temporal lobe epilepsy.

Epilepsy &amp; behavior : E&amp;B
2021

Isolated cortical tuber in an infant with genetically confirmed tuberous sclerosis complex 1 presenting with symptomatic West syndrome.

Neuropathology : official journal of the Japanese Society of Neuropathology
2020

Unsupervised machine learning reveals lesional variability in focal cortical dysplasia at mesoscopic scale.

NeuroImage. Clinical
2020

Oligodendrocyte lineage and myelination are compromised in the gray matter of focal cortical dysplasia type IIa.

Epilepsia
2019

Reelin, tau phosphorylation and psychiatric complications in patients with hippocampal sclerosis and structural abnormalities in temporal lobe epilepsy.

Epilepsy &amp; behavior : E&amp;B
2019

Prevalence and clinical characteristics of malformations of cortical development and incomplete hippocampal inversion with medically intractable seizures in Chennai - A prospective study.

Neurology India
2018

Histopathology of 3 Tesla MRI-negative extratemporal focal epilepsies.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
2018

Surgical outcome and predictive factors of epilepsy surgery in pediatric isolated focal cortical dysplasia.

Epilepsy research
2017

[Neuropathologic findings in intractable epilepsy: a clinicopathologic analysis of 822 cases].

Zhonghua bing li xue za zhi = Chinese journal of pathology
2017

Putting the new ILAE classification of focal cortical dysplasia into practice in western China.

Seizure
2017

A distinct clinicopathological variant of focal cortical dysplasia IIId characterized by loss of layer 4 in the occipital lobe in 12 children with remote hypoxic-ischemic injury.

Epilepsia
2018

Childhood-Onset Epileptic Encephalopathy Associated With Isolated Focal Cortical Dysplasia and a Novel TSC1 Germline Mutation.

Clinical EEG and neuroscience
2017

Induced pluripotent stem cells from patients with focal cortical dysplasia and refractory epilepsy.

Molecular medicine reports
2016

Focal cortical dysplasia: Molecular disturbances and clinicopathological classification (Review).

International journal of molecular medicine
2017

Temporal lobe epilepsy and focal cortical dysplasia in children: A tip to find the abnormality.

Epilepsia
2016

Pathology-Based Approach to Seizure Outcome After Surgery for Pharmacoresistant Medial Temporal Lobe Epilepsy.

World neurosurgery
2016

Short- and long-term surgical outcomes of temporal lobe epilepsy associated with hippocampal sclerosis: Relationships with neuropathology.

Epilepsia
2015

Comparison of electrocorticographic patterns with focal cortical dysplasia types in children with epilepsy.

Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko
2015

Evidence for the involvement of gamma delta T cells in the immune response in Rasmussen encephalitis.

Journal of neuroinflammation
2015

Cytochrome c oxidase deficit is associated with the seizure onset zone in young patients with focal cortical dysplasia Type II.

Metabolic brain disease
2015

Failure to detect human papillomavirus in focal cortical dysplasia type IIb.

Annals of neurology
2015

Focal cortical dysplasias in temporal lobe epilepsy surgery: Challenge in defining unusual variants according to the last ILAE classification.

Epilepsy &amp; behavior : E&amp;B

Associações

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Doença com base genética

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Conselhos e sociedades

Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Ainda não achamos doenças com sintomas parecidos o suficiente.

Perguntas frequentes

O que as famílias mais perguntam sobre esta doença — cada resposta com a fonte de onde saiu

Respostas geradas por IA a partir das fontes citadas

A condição apresenta relação conhecida com variantes no gene **SLC35A2**, o qual codifica a proteína transportadora UDP-galactose translocator. Além disso, pesquisas médicas investigam mutações somáticas presentes diretamente no tecido cerebral afetado.

Referências

Fontes citadas no texto, publicações do grafo e bases de dados usadas neste verbete

3 fontes citadas no texto · 10 publicações do grafo RarasNet (PubMed) · 5 bases de dados. Títulos, periódicos e PMIDs vêm direto da fonte, sem intermediação de IA.

  1. MONDO
    purl.obolibrary.org
  2. Isolated hippocampal sclerosis and focal dysplasia type IIIa: Comparative study of anatomo-electro-clinical profile and seizure outcome.
    Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology2026PMID 41352305
  3. Identifying the epileptogenic zone by 18F-FDG PET/MRI in drug-resistant epilepsy with focal cortical dysplasia type IIIa.
    Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology2026PMID 41232484
  4. GARD:20983
    GARD (NIH)
  5. Q55786806
    Wikidata

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Citar este verbete

Raras. (2026). Displasia cortical focal isolada tipo I. Em Raras — Enciclopédia de Doenças Raras do Brasil. https://raras.org/doenca/displasia-cortical-focal-isolada-tipo-i

Formato APA. Conteúdo sob CC BY 4.0 — reuso livre com atribuição.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Compêndio · Raras BR

Displasia cortical focal isolada tipo I

ORPHA:268961 · MONDO:0017095
🇧🇷 Brasil SUS
SIGTAP
5 procedimentos
Geral
Prevalência
Unknown
CID-10
Q04.8 · Outras malformações congênitas especificadas do encéfalo
CID-11
Prevalência
0.0 (Worldwide)
MedGen
UMLS
C5679772
EuropePMC
Wikidata
Papers 10a

📋 Origem dos dados

Esta página agrega dados de fontes públicas e oficiais. Dados sobre cobertura no SUS (PCDT, CEAF) são verificados ativamente por agente proativo (ver badge no infobox). Demais dados têm atribuição de fonte + data da última sincronização — clique para abrir o original.

Doença rara (ontologia)
fonte: Orphanet
Identificador unificado
fonte: MONDO
Dado público estruturado
fonte: Wikidata
Rara