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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...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Kibret Enyew Belay, Beza Leulseged Ayalew, Melaku Taye Amogne, Theodros Aberra Alemneh, Tedla Kebede Geletew
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMC 2023-12-01
Schriftenreihe:Journal of Medical Case Reports
Schlagworte:
Prader–Willi
Ethiopia
Obesity
Case report
Hypogonadism
Online-Zugang:https://doi.org/10.1186/s13256-023-04282-5
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