GENERALIZED OSTEOPOROSIS IN A PATIENT WITH OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME (OOCHS), WITHOUT CEREBRAL DEFECTS - A NEW SYNDROME

Authors
HERNANDEZ A NAZARA Z REYNOSO MC SARRALDE A BOBADILLA L FRAGOSO R
Citation
A. Hernandez et al., GENERALIZED OSTEOPOROSIS IN A PATIENT WITH OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME (OOCHS), WITHOUT CEREBRAL DEFECTS - A NEW SYNDROME, Clinical genetics, 49(1), 1996, pp. 46-48
Citations number
10
Categorie Soggetti
Genetics & Heredity
Journal title
Clinical genetics → ACNP
ISSN journal
00099163
Volume
49
Issue
1
Year of publication
1996
Pages
46 - 48
Database
ISI
SICI code
0009-9163(1996)49:1<46:GOIAPW>2.0.ZU;2-6
Abstract
An 8-year-old male patient presented a unique pattern of congenital an omalies. Prominent findings included a combination of severe osteoporo sis and congenital oculocutaneous hypopigmentation. The patient may re present a hitherto undescribed syndrome of unknown etiology.