Review began 12/15/2022 review ended 12/21/2022 published 12/23/2022 © copyright

HIGHLIGHTS

• who: Report and colleagues from the (UNIVERSITY) have published the research work: Review began 12/15/2022 Review ended 12/21/2022 Published 12/23/2022 u00a9 Copyright, in the Journal: (JOURNAL) of December/23,/2022
• what: Alstru00f6m syndrome is a rare genetic disorder caused by mutations in the ALMS1 gene.

SUMMARY

Alström syndrome is a rare autosomal recessive genetic disorder. One of the most common symptoms is cone-rod dystrophy leading to visual loss, with others being hearing loss and cardiomyopathy. Forty percent (40%) of children with Alström . . .

 



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