منابع مشابه
Human Intersex
London: E. & S. Livingstone, 1962. THE extraordinar-y developmenit of research aInd increase in knowledge of sexual alnomalies and human genetics, in the last decade, has outdistaniced most clinicians leavinlg us sadly bewildered. The steady outpouring of papers has literally svamped us aIId if we are to gain any insight into this rapidly increasing field of medical understanding Nve are depeni...
متن کاملHypophysis and Hypothalamus
3 Diseases ................................................................................. 17 3.1 Anterior Pituitary Deficiency................................................ 17 3.2 Central Diabetes Insipidus .................................................... 21 3.3 Precocious or Delayed Puberty............................................. 23 3.4 Other Endocrinopathies .......................
متن کاملTrisomy 22 and intersex.
Complete trisomy 22, with or without mosaicism, has been reported as a distinct syndrome. In this report an infant is described who was externally male but with female rudimentary internal organs and whose karyotype was 47,XX+22.
متن کاملAmbiguous genitalia and intersex.
Intersex disorders are rare congenital malformations with over 80% being diagnosed with congenital adrenal hyperplasia (CAH). It can be challenging to determine the correct gender at birth and a detailed understanding of the embryology and anatomy is crucial. The birth of a child with intersex is a true emergency situation and an immediate transfer to a medical center familiar with the diagnosi...
متن کاملThe new Science of Intersex
R. JOneS was surprisingly relaxed and jovial considering that he had driven two hours from Bakersfield to Los Angeles to have his thirteen-month-old child examined by half a dozen doctors. no doubt he was sustained by his faith: on his T-shirt was boldly emblazoned “Got Jesus?” The examination rooms are usually crowded in the Intersex Clinic (now the Disorders of Sex Development [DSD] Clinic) a...
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ژورنال
عنوان ژورنال: The Japanese Journal of Genetics
سال: 1942
ISSN: 0021-504X,1880-5787
DOI: 10.1266/jjg.18.115