A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid Paralysis.

Gowda, Vykuntaraju K; Kerur, Chetan; Vamyanmane, Dhananjaya K; Kumar, Pragalatha; Nagarajappa, Vani H; Shivappa, Sanjay K

Gowda, Vykuntaraju K; Kerur, Chetan; Vamyanmane, Dhananjaya K; Kumar, Pragalatha; Nagarajappa, Vani H; Shivappa, Sanjay K.

Afiliação

Gowda VK; Department of Pediatric Neurology, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
Kerur C; Department of Pediatrics, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
Vamyanmane DK; Department of Radiology, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
Kumar P; Department of Pediatrics, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
Nagarajappa VH; Department of Pediatrics, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
Shivappa SK; Department of Pediatrics, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.

J Pediatr Genet ; 11(3): 257-260, 2022 Sep.

Article em En | MEDLINE | ID: mdl-35990026

Palavras-chave

acute flaccid paralysis; biotinidase deficiency; demyelination; inborn errors of metabolism; spinal cord

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Pediatr Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia

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