Evaluation of 4-month-old girl who presented with congenital cataracts revealed heterochromia iridis, fundus hypopigmentation, residual white forelock and sensory neural hearing loss - findings ...

In the present study, three affected patients (I-2, II-2, III-1) and one unaffected member (I-1) from an isolated village in Inner Mongolia in China were involved in our study (Figure 1a). The proband ...

With the X-ray vision of DESY's light source DORIS, a research team from Hamburg and Iceland has uncovered the molecular structure of a master regulator central to the most deadly form of skin cancer, ...

Beth Leipholtz from Minnesota is candid about her son living with Waardenburg syndrome. It's a genetic condition that affects the coloring of skin, hair, and eyes, according to the Cleveland Clinic.

The first African case of Waardenburg's syndrome is described, presenting with the usual features of the syndrome, and in addition some features not reported before.

SYRACUSE N.Y. — A family in Syracuse is counting their blessings this holiday season, as they celebrate a medical breakthrough for their baby girl. 9-month-old Aida Little was born with Waardenburg ...

Successful treatment of hidradenitis suppurativa with rituximab for a patient with idiopathic carpotarsal osteolysis and chronic active antibody-mediated rejection. Waardenburg syndrome type IIE in a ...