A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report

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作者：
Asanka Rathnasiri
Udara Senarathne
Visvalingam Arunath
Thabitha Hoole
Ishara Kumarasiri
Oshanie Muthukumarana
Eresha Jasinge
Sachith Mettananda
机构：
[1] Colombo North Teaching Hospital,Department of Biochemistry, Faculty of Medical Sciences
[2] University of Sri Jayewardenepura,Department of Paediatrics, Faculty of Medicine
[3] Lady Ridgeway Children’s Hospital,undefined
[4] University of Kelaniya,undefined
来源：
BMC Endocrine Disorders | / 21卷
关键词：
Contiguous gene deletion syndrome; Congenital adrenal hypoplasia; Duchenne muscular dystrophy; Glycerol kinase deficiency;
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