BACKGROUND AND PURPOSE: Woodhouse-Sakati syndrome is a rare autosomal
recessive disorder characterized by hypogonadism, alopecia, diabetes mellitus, and …

Abstract Woodhouse–Sakati Syndrome is a very rare autosomal recessive disorder caused
by pathogenic variants in the DCAF17 gene, which encodes DDB1‐and CUL4‐associated …

Objective: Rare disease Background: Woodhouse-Sakati syndrome (WSS) is a rare
autosomal recessive genetic condition that was first described in 1983. Since its original …

Abstract First described in 1983, Woodhouse-Sakati syndrome (WSS) is a rare autosomal
recessive genetic disorder that leads to a spectrum of hypogonadal symptoms in …

Woodhouse-Sakati syndrome (WSS) is a rare genetic condition of autosomal recessive
inheritance pattern. The disease is characterized by a group of disorders, including diabetes …

Abstract Background Woodhouse-Sakati syndrome (WSS)(OMIM# 241080) is an extremely
rare multisystemic disease. Alopecia, hypogonadism, loss of hearing, hypothyroidism …

Woodhouse-Sakati syndrome is a rare genetic syndrome caused by homozygous mutations
of the DCAF17 gene. Several endocrine organs may be affected in the course of the …

Woodhouse‐Sakati syndrome (WSS) is a rare autosomal recessive neuroendocrine and
ectodermal disorder caused by variants in the DCAF17 gene. In Qatar, the c. 436delC …

Hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal
syndrome [also known as Woodhouse–Sakati syndrome (WSS)] is a rare autosomal …

Abstract Background and Objective: Woodhouse-Sakati syndrome (WSS) is a rare
autosomal-recessive disorder characterized by a combination of hypogonadism, alopecia …