17-α-Hydroxylase deficiency: An unusual case with primary amenorrhea and hypertension
A 14-year-old girl presented with acute onset quadriparesis and newly detected hypertension. Parental consanguinity, delayed puberty with normal stature form the additional information. Hypokalemia with metabolic alkalosis, low cortisol, high ACTH and FSH pointed to the possibility of CAH with 17α h...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Wolters Kluwer Medknow Publications
2011-01-01
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| Σειρά: | Indian Journal of Endocrinology and Metabolism |
| Θέματα: | |
| Διαθέσιμο Online: | http://www.ijem.in/article.asp?issn=2230-8210;year=2011;volume=15;issue=2;spage=127;epage=129;aulast=Kota |
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