waardenburg syndrome - Axtarish в Google
16 авг. 2022 г. · Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, ...
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, ...
Синдром Ваарденбурга Заболевание
Синдром Ваарденбурга — наследственное заболевание. Имеет следующие клинические признаки: телекант, гетерохромия радужки, седая прядь надо лбом и врождённая тугоухость различной степени. Википедия
МКБ-10 : E70.3 ( ILDS E70.32)
МКБ-9 : 270.2
Waardenburg syndrome is a group of conditions passed down through families. The syndrome involves deafness and pale skin, hair, and eye color.
15 авг. 2022 г. · Waardenburg syndrome is a genetic condition that affects the coloring (pigmentation) of your skin, hair and eyes.
Waardenburg syndrome is a genetic disorder that may be evident at birth (congenital). The range and severity of associated symptoms and findings may vary ...
Waardenburg syndrome (WS) is a group of genetic conditions characterized by varying degrees of hearing loss and differences in the coloring (pigmentation) ...
A rare genetic multiple congenital anomalies characterized by deafness and defects in neural crest-derived structures, including pigmentation anomalies of the ...
Waardenburg syndrome is a rare genetic disorder characterised by sensorineural hearing loss and pigmentary abnormalities of the hair, skin, and eyes.
Waardenburg syndrome refers to several rare genetic conditions that cause hearing loss, changes in the color of the eyes, skin, and hair, and changes in the ...
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