Study to assess the knowledge of caretakers regarding corticosteroid therapy in children with congenital adrenal hyperplasia – 21 hydroxylase deficiency

Background: The primary aim of treating congenital adrenal hyperplasia (CAH) due to 21 hydroxylase deficiency is to replace the deficient glucocorticoids and mineralocorticoids, to minimize the excess androgen production and to facilitate normal growth. Children with CAH require daily treatment life...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Vasantha Singarayan, Anita David, Vageesh Ayyar, Saji James
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Wolters Kluwer Medknow Publications 2020-01-01
Σειρά:	Journal of Family Medicine and Primary Care
Θέματα:	21 hydroxylase deficiency congenital adrenal hyperplasia parenting steroid therapy
Διαθέσιμο Online:	http://www.jfmpc.com/article.asp?issn=2249-4863;year=2020;volume=9;issue=6;spage=2814;epage=2817;aulast=
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