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Teaching NeuroImages: Trigeminal Ganglia Hypoplasia as Imaging Clue for the Diagnosis of Gómez-López-Hernández Syndrome.
Perrone, Eduardo; Burlin, Stênio; D'Almeida, Vânia; Alvarez Perez, Ana Beatriz; Lygia de Macena Sobreira, Nara; Procaci, Victor Rebelo; Avelino Jacobina, Marcela Amaral; Barsottini, Orlando G; Pedroso, José Luiz.
Afiliação
  • Perrone E; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Burlin S; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • D'Almeida V; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Alvarez Perez AB; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Lygia de Macena Sobreira N; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Procaci VR; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Avelino Jacobina MA; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Barsottini OG; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
  • Pedroso JL; From the Department of Clinical Genetics (E.P., A.B.A.P.), Department of Radiology (S.B.), Department of Pediatrics and Psychobiology (V.D., M.A.A.J.), and Ataxia Unit, Department of Neurology (V.R.P., O.G.B., J.L.P.), Universidade Federal de São Paulo, Brazil; and Department of Clinical Genetics (N
Neurology ; 96(11): e1593-e1594, 2021 03 16.
Article em En | MEDLINE | ID: mdl-33168701
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cerebelo / Gânglio Trigeminal / Anormalidades Craniofaciais / Síndromes Neurocutâneas / Alopecia / Transtornos do Crescimento Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cerebelo / Gânglio Trigeminal / Anormalidades Craniofaciais / Síndromes Neurocutâneas / Alopecia / Transtornos do Crescimento Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article