cardio-facio-cutaneous syndrome - Axtarish в Google
Cardiofaciocutaneous (CFC) syndrome is one of the RASopathies and is a rare genetic disorder is typically characterized by unusually sparse, brittle, curly hair; relatively large head (relative macrocephaly); a prominent forehead and abnormal narrowing of the sides of the forehead (bi-temporal narrowing); intellectual ...
28 мар. 2022 г. · Cardiofaciocutaneous syndrome is a disorder that affects many parts of the body, particularly the heart (cardio-), facial features (facio-), ...
18 янв. 2007 г. · Cardiofaciocutaneous (CFC) syndrome is characterized by cardiac abnormalities (pulmonic stenosis and other valve dysplasias, septal defects, hypertrophic ...
Common features of CFC syndrome include congenital heart disease, characteristic facial features and skin abnormalities.
Cardiofaciocutaneous (CFC) syndrome is an extremely rare genetic disorder, and is one of the RASopathies. It was first described in 1986.
A rare, multiple congenital anomalies syndrome characterized by craniofacial dysmorphology, congenital heart disease, dermatological abnormalities (most ...
CFC syndrome is a disorder involving heart defects and abnormalities of the face, skin and hair. It often involves intellectual disability and growth ...
CFC is genetically heterogeneous and caused by gene mutations in the Ras/mitogen-activated protein kinase pathway. The major features of CFC include ...
Cardiofaciocutaneous (CFC) syndrome is a rare genetic condition. It affects the heart, facial features, and skin.
Cardio refers to changes in the structure and/or function of the heart, facio to distinctive facial features, and cutaneous to changes seen in the skin, hair ...
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