Overview

Bardet-Biedl syndrome and Laurence-Moon syndrome are rare autosomal recessive disorders that share a similar clinical phenotype. These syndromes are characterized by progressive features including cone-rod retinal dystrophy, obesity, and hypogonadism in males. Additional clinical manifestations can include learning disabilities, renal abnormalities, and polydactyly. Despite their similarities, Bardet-Biedl syndrome and Laurence-Moon syndrome are distinguished by certain clinical features. This book describes the management of the ocular manifestations of Bardet-Biedl syndrome through new evidence-based therapies.The current treatment options are not curative; they may help slow progression and preserve vision. The combination of citicoline, goji berry, coenzyme Q10, and lutein represents a promising approach for the management of retinal degeneration in BBS patients, though further clinical trials are needed to confirm their efficacy.

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