Osteoporosis-oculocutaneous hypopigmentation syndrome

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

Also known as: Hernández-Fragoso syndrome, OOCHS, OOCH, OOCH syndrome, osteoporosis and oculocutaneous hypopigmentation syndrome, osteoporosis oculocutaneous hypopigmentation syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Osteoporosis-oculocutaneous hypopigmentation syndrome itself.