Biotinidase deficiency

*Gene map locus 3p25

BTD deficiency

Multiple carboxylase deficiency, juvenile-onset

Multiple carboxylase deficiency, late-onset

[Clinical features: neurological, dermatological, immunological, and ophthalmological abnormalities]

[Inheritance: autosomal recessive]


Biotinidase deficiency	Biotinidase deficiency	Biotinidase Deficiency with Hypertonia as Unusual Feature
Indian Pediatrics	Indian Pediatrics	Indian Pediatrics


Biotinidase Deficiency with Hypertonia as Unusual Feature
Indian Pediatrics

Search with keyword(s) And Or Wildcard = *


Print this page

Edited by Aldo Campana, February 8, 2010