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...
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) |
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Format: | Article |
Language: | English |
Published: |
BioMed Central Ltd
2022
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Subjects: | |
Online Access: | View Fulltext in Publisher |
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