Related Experiment Videos

Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old child

M O Rolland¹, P Divry, M T Zabot

¹Centre d'Etude des Maladies Métaboliques, Hôpital Debrousse, Lyon, France.

Journal of Inherited Metabolic Disease

|January 1, 1991

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Characteristics and outcomes of patients with pediatric-onset non-mastocytosis mast cell activation disorders: A CEREMAST study.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology·2026

Epidemiology, clinical features, and mortality rate of Wilson disease in Moroccan children: A pediatric case series.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2022

Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study.

Clinical and translational gastroenterology·2018

TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature review.

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2018

Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategy.

Clinical genetics·2018

[Compliance with treatment in Wilson's disease: On the interest of a multidisciplinary closer follow-up].

La Revue de medecine interne·2017

See all related articles