AB031. Disorders of sex development: a clinical profile from Palembang, Indonesia
نویسندگان
چکیده
منابع مشابه
Disorders of Sex Development
The birth of a new baby is one of the most dramatic events in a family, and the first question is usually "is it a boy or a girl?" The newborn infant with ambiguous external genitalia often comes as a surprise for the doctors as well as the parents and is sometimes described as an endocrine emergency situation presenting a problem of sex assignment. The nomenclature such as 'intersex', 'hermaph...
متن کاملDisorders of sex development
a Canakkale Onsekiz Mart University, Medical Faculty, Department of Urology, Canakkale, Turkey b Inönü University, Medical Faculty, Department of Urology, Malatya, Turkey c Canakkale Onsekiz Mart University, Medical Faculty, Department of Children Disease, Canakkale, Turkey d Canakkale Onsekiz Mart University, Medical Faculty, Department of Obstetric and Gynecology, Canakkale, Turkey e Canakkal...
متن کاملDisorders of Sex Development
Introduction Sexual differentiation is the process of development of the differences between male and female from an undifferentiated zygote (fertilised egg). Sex and gender are both important determinants of health. The term “gender” describes those characteristics of females and males that are largely socially created, whereas “sex” encompasses those characteristics that are biologically dete...
متن کاملDisorders of Sex Development (sds): New Concepts, and Clinical Management
The disorders of sex development constitute a serious and complex clinical problem requiring the participation of a multidisciplinary team for adequate management of urgencies and long-term follow up. In recent years, the advancement of molecular genetics has generated important advances in our knowledge of these disorders. A landmark in this subject has been the publication of a Consensus Stat...
متن کاملEtiology and clinical profile of children and adolescents with disorders of sex development (DSD) presenting with ambiguous external genitalia
Results 42 patients (age-neonate to 18 years, 14 (46 XX DSD), 26(46XY DSD) and 2(sex chromosome DSD) were evaluated.46 XX DSD was due to Congenital Adrenal Hyperplasia (CAH) (12/14) and SyndromicDSD(2/14). All presented with clitoromegaly and labioscrotal fusion. 5/12presented in infancy, with Adrenal crisis and severe (prader stage ≥3) virilization(Salt Wasting CAH), 7 had Simple VirilizingCAH...
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ژورنال
عنوان ژورنال: Annals of Translational Medicine
سال: 2017
ISSN: 2305-5839,2305-5847
DOI: 10.21037/atm.2017.s031