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Hemimegalencephaly with Bannayan-Riley-Ruvalcaba syndrome.
Ghusayni, Ryan; Sachdev, Monisha; Gallentine, William; Mikati, Mohamad A; McDonald, Marie T.
Afiliação
  • Ghusayni R; Division of Pediatric Neurology, Department of Pediatrics, Duke University, Durham.
  • Sachdev M; Division of Pediatric Neurology, Department of Pediatrics, Duke University, Durham.
  • Gallentine W; Division of Pediatric Neurology, Department of Pediatrics, Duke University, Durham.
  • Mikati MA; Division of Pediatric Neurology, Department of Pediatrics, Duke University, Durham.
  • McDonald MT; Division of Medical Genetics, Department of Pediatrics, Duke University, Durham, USA.
Epileptic Disord ; 20(1): 30-34, 2018 Feb 01.
Article em En | MEDLINE | ID: mdl-29444762
Hemimegalencephaly is known to occur in Proteus syndrome, but has not been reported, to our knowledge, in the other PTEN mutation-related syndrome of Bannayan-Riley-Ruvalcaba. Here, we report a patient with Bannayan-Riley-Ruvalcaba syndrome who also had hemimegalencephaly and in whom the hemimegalencephaly was evident well before presentation of the characteristic manifestations of Bannayan-Riley-Ruvalcaba syndrome. An 11-year-old boy developed drug-resistant focal seizures on the fifth day of life. MRI revealed left hemimegalencephaly. He later showed macrocephaly, developmental delay, athetotic quadriplegic cerebral palsy, and neuromuscular scoliosis. Freckling of the penis, which is characteristic of Bannayan-Riley-Ruvalcaba syndrome, was not present at birth but was observed at 9 years of age. Gene analysis revealed a c.510 T>G PTEN mutation. This patient and his other affected family members, his father and two siblings, were started on the tumour screening procedures recommended for patients with PTEN mutations. This case highlights the importance of early screening for PTEN mutations in cases of hemimegalencephaly not otherwise explained by another disorder, even in the absence of signs of Proteus syndrome or the full manifestations of Bannayan-Riley Ruvalcaba syndrome.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Hamartoma Múltiplo / PTEN Fosfo-Hidrolase / Hemimegalencefalia Limite: Child / Humans / Male Idioma: En Revista: Epileptic Disord Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Hamartoma Múltiplo / PTEN Fosfo-Hidrolase / Hemimegalencefalia Limite: Child / Humans / Male Idioma: En Revista: Epileptic Disord Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos