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
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 group of conditions passed down through families. The syndrome involves deafness and pale skin, hair, and eye color.
Waardenburg syndrome is a group of genetic conditions inherited in an autosomal dominant fashion. During embryogenesis, there is an abnormal distribution of ...
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) ...
Waardenburg syndrome is a rare genetic disorder characterised by sensorineural hearing loss and pigmentary abnormalities of the hair, skin, and eyes.
16 нояб. 2020 г. · Mutations in the genes PAX3 and MITF have been described in WS, which is clinically characterized by congenital hearing loss and pigmentation anomalies.
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