A 14-year-old male patient with diagnosis of Prader–Willi syndrome in Ethiopia: a case report

Abstract Background Prader–Willi syndrome is a complex multisystem disorder due to the absent expression of paternally active genes in the Prader–Willi syndrome-critical region on chromosome 15 (15q11.2-q13). The main clinical features are hyperphagia (which frequently results in early-onset obesity...

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Principais autores:	Kibret Enyew Belay, Beza Leulseged Ayalew, Melaku Taye Amogne, Theodros Aberra Alemneh, Tedla Kebede Geletew
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2023-12-01
coleção:	Journal of Medical Case Reports
Assuntos:	Prader–Willi Ethiopia Obesity Case report Hypogonadism
Acesso em linha:	https://doi.org/10.1186/s13256-023-04282-5
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