Bardet–Biedl syndrome: a case series

Bardet–Biedl syndrome: a case series

Background: Bardet–Biedl syndrome is a rare multisystem autosomal recessive disorder that falls under the spectrum of ciliopathy disorders. It is characterized by rod–cone dystrophy, renal malformations, polydactyly, learning difficulties, central obesity, and hypogonadism. Many minor features that...

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Main Authors: Abdalla, S.M.A (Author), Abu Shama, E.A.E (Author), Ahmed, M.M.M (Author), Albashir, A.A.D (Author), Ali, H.I.H (Author), Dafallah, M.A (Author), Daw Elbait, A.A.E (Author), Elawad, O.A.M.A (Author), Mohammed, M.A.Y (Author), Mohammed, M.E (Author), Mohammed, N.F.N (Author), Osman, F.H.M (Author), Yousif, H.H.M (Author)
Format: Article
Language:English
Published: BioMed Central Ltd 2022
Subjects:
Bardet–Biedl syndrome
Cilioapathy
Sudan
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