A rare case of complete androgen insensitivity syndrome in a 13-year-old lebanese child, reared as female, with bilateral inguinal hernia

HIGHLIGHTS

• who: Stephanie Farah from the (UNIVERSITY) have published the Article: A rare case of complete androgen insensitivity syndrome in a 13-year-old Lebanese child, reared as female, with bilateral inguinal hernia, in the Journal: (JOURNAL)
• what: The authors report a homozygous mutation p.R856C (c.2566C>T) in exon 7 of the AR gene in a case of complete androgen insensitivity with history of inguinal hernia during infancy.

SUMMARY

Reports of coexistence of Kallmann syndrome and complete androgen insensitivity syndrome were reported in two sisters from Lebanese consanguineous parents. Given . . .

 



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