Osteoporosis oculocutaneous hypopigmentation syndrome

Alternate names[edit | edit source]

OOCH; OOCH syndrome

Definition[edit | edit source]

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.

NIH genetic and rare disease info[edit source]

NIH info on Osteoporosis oculocutaneous hypopigmentation syndrome

Osteoporosis oculocutaneous hypopigmentation syndrome is a rare disease.

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