Aarskog syndrome is a rare and inherited disease associated with short stature, typical facial and digital features and shawl scrotum. Here, we report a female 14.5 year-old Aarskog syndrome case, with short stature, dysmorphic facial features, brachydactyly and congenital heart disease (CHD).She and her mother with similar clinical features are presented as females with clinical features are very rare
Field : Sağlık Bilimleri
Journal Type : Uluslararası
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