Aug 14, 2023 · People with Woodhouse-Sakati syndrome produce abnormally low amounts of hormones that direct sexual development (hypogonadism), which typically ...

Aug 4, 2016 · Type 1. Severe and progressive neurologic disability at a younger age (range 9-17 years) causing significant impairment of the quality of life ...

Woodhouse–Sakati syndrome, is a rare autosomal recessive multisystem disorder which causes malformations throughout the body, and deficiencies affecting the ...

Hypoparathyroidism-short stature-intellectual disability-seizures syndrome; Richardson-Kirk syndrome; SSS. Prevalence: Unknown. Inheritance: Autosomal recessive.

Sanjad-Sakati Syndrome is a rare genetic condition characterized by growth delay, intellectual disability, and other symptoms. Early diagnosis and treatment can ...

Woodhouse Sakati syndrome is categorized by DM, intellectual disability, hearing loss, hypothyroidism, hypogonadism, and alopecia. Electrocardiogram anomalies ...

Sanjad–Sakati syndrome (Middle East syndrome) is a rare autosomal recessive genetic condition seen in offspring of Middle Eastern origin.

Feb 20, 2024 · Woodhouse-Sakati syndrome is a rare autosomal recessive genetic disorder characterized by neurodegeneration resulting from mutations in the ...

Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs ...