Secondary diabetes mellitus in Prader-Willi syndrome

Objective Prader-Willi Syndrome (PWS) is a rare autosomal dominant disorder on the 15q11.2-q13 chromosome. PWS may impact metabolic, endocrine, and neurologic systems and combine with hypotonia, sleep disturbances, cognitive disability, central adrenal insufficiency, hypothyroidism, hypogonadism, sh...

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Veröffentlicht in:	International journal of diabetes in developing countries 2021-10, Vol.41 (4), p.683-687
Hauptverfasser:	Gao, Chuqi, Yao, Xiaoli, Liu, Juan
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report Case reports Children Chromosome 15 Cognitive ability Diabetes Diabetes mellitus Differential diagnosis Family Medicine General Practice Growth hormones Health Administration Hereditary diseases Hypogonadism Hypothyroidism Medicine Medicine & Public Health Neonates Patients Prader-Willi syndrome
Online-Zugang:	Volltext
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