Biotinidase deficiency in a newborn-Reference-Cited by-同舟云学术

Biotinidase deficiency in a newborn

Published:2020-04-10 Issue:1 Volume:13 Page:139-141
ISSN:1934-5798
Container-title:Journal of Neonatal-Perinatal Medicine
language:
Short-container-title:NPM

Author:

El Moussaoui S.¹²,Bennaoui F.¹²,El Idrissi Slitine N.¹²,Houcar O.³,Maoulainine F.M.R.¹²

Affiliation:

1. Neonatal Intensive Care Unit, Mother and Child Hospital, Mohammed VI University Hospital, Marrakesh, Morocco

2. Childhood Health and Development Research Team, Marrakech Medical School, Cadi Ayyad University, Marrakesh, Morocco

3. Department of Dermatology, Mohammed VI Marrakech University Hospital, Marrakesh, Morocco

Publisher

IOS Press

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Wolf B . Disorders of biotin metabolism. In: The Metabolic and Molecular Bases of Inherited Disease 8th ed. Scriver CR , Beaudet AL , Sly WS , eds. New York: McGraw-Hill 2001:3935–62.

2. Newborn screening in India;Rama Devi;Indian J Pediatr,2004

3. Biotinidase deficiency;Dahiphale;Indian Pediatr,2008

4. Biotinidase deficiency with hypertonia as unusual feature;Rathi;Indian Pediatr,2009

5. Biotinidase deficiency: A survey of 10 cases;Wastell;Arch Dis Child,1988

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2. Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures;Annals of Child Neurology;2024-01-01

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