Bardet–Biedl syndrome and related disorders in Japan View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2020-05-25

AUTHORS

Makito Hirano, Wataru Satake, Nobuko Moriyama, Ken Saida, Nobuhiko Okamoto, Pei-Chieng Cha, Yutaka Suzuki, Susumu Kusunoki, Tatsushi Toda

ABSTRACT

Bardet–Biedl syndrome (BBS) is a rare autosomal recessive disorder characterized by obesity, mental impairment, rod-cone dystrophy, polydactyly, male hypogonadism, and renal abnormalities. This disorder is caused by mutations in BBS1-21. Alström syndrome (AS), caused solely by mutations in ALMS1, is another genetic obesity syndrome clinically similar to BBS. We previously conducted the first nationwide survey of BBS in Japan and found four patients with genetically definite BBS. In this study, exome analyses were performed on new patients whose symptoms fulfilled the diagnostic criteria for BBS. We identified one reported heterozygous mutation in BBS1 (p.R429*) in one patient, two novel mutations (p.L493R and p.H719Y) in BBS20 in a second patient, and one novel mutation (p.Q920*) and one reported mutation (p.R2928*) in ALMS1 in a third patient, who was subsequently diagnosed with AS. The first patient with BBS was previously considered to have digenic heterozygous mutations in BBS1 and BBS4. RT-PCR and long-range genomic PCR analyses identified a new heterozygous mutation in BBS1, the deletion of exons 10 and 11. Thus, this patient was compound heterozygous for mutations in BBS1. Many studies have described digenic heterozygous mutations in BBS. However, undetected mutations might have existed in either one of the mutated genes. More... »

PAGES

847-853

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s10038-020-0778-y

DOI

http://dx.doi.org/10.1038/s10038-020-0778-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1127868096

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/32451492


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