Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Article in English | IMSEAR | ID: sea-156324

ABSTRACT

Biotinidase deficiency is a rare metabolic disorder which can cause dermatological manifestations and lead to severe neurological sequelae if untreated. Holocarboxylase synthetase deficiency also has similar manifestations and needs to be differentiated. We present a neonate who had atypical early onset symptoms and was diagnosed to have biotinidase deficiency.


Subject(s)
Alopecia/etiology , Biotinidase Deficiency/complications , Biotinidase Deficiency/diagnosis , Biotinidase Deficiency/genetics , Fatal Outcome , Female , Humans , Ichthyosis/etiology , Infant, Newborn , Seizures/etiology
SELECTION OF CITATIONS
SEARCH DETAIL