📂 Diseases
short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome — Definition
Kısa boy-tırnak displazisi-yüz dismorfisi-hipotrikoz sendromu / short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
Rarely seen is a genetic disease, characterized by short size as a result of prenatal and post-natal growth recovery. Figure disorder (displasia), pronounced facial abnormalities (dismorphi) and rare hair, eyebrows, hair failure (hypotricosis). Otozomal indicates resesif inheritance and does not usually accompany intelligence backrest.
Frequently Asked Questions
❓ What is Kısa boy-tırnak displazisi-yüz dismorfisi-hipotrikoz sendromu?
Kısa boy-tırnak displazisi-yüz dismorfisi-hipotrikoz sendromu; rarely seen is a genetic disease, characterized by short size as a result of prenatal and post-natal growth recovery. Figure disorder (displasia), pronounced facial abnormalities (dismorphi) and rare hair, eyebrows, hair failure (hypotricosis). Otozomal indicates resesif inheritance and does not usually accompany intelligence backrest.
❓ What is short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome in Turkish?
The Turkish equivalent of "short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome" is Kısa boy-tırnak displazisi-yüz dismorfisi-hipotrikoz sendromu.
❓ Which medical field is Kısa boy-tırnak displazisi-yüz dismorfisi-hipotrikoz sendromu related to?
This term belongs to the Diseases category.