Osteoporosis-Oculocutaneous Hypopigmentation Syndrome

Watchlist
Retrieved
2021-01-23
Source
Trials
Genes
Drugs

Osteoporosis-oculocutaneous hypopigmentation syndrome is characterised by osteoporosis and congenital oculocutaneous hypopigmentation. Three cases have been described in the literature. The mode of inheritance appears to be autosomal recessive.