| Literature DB >> 24400298 |
Abstract
Congenital adrenal hyperplasia (CAH) most commonly due to 21-hydroxylase deficiency is the most common type of disorder of sex development. This review will focus on CAH addressing historical and current surgical techniques with their anatomical foundations, with special attention to long-term results and outcomes on sexual function, patient satisfaction, patient attitude toward surgery, and ongoing controversies in management of these patients.Entities:
Keywords: 21-hydroxylase deficiency; clitoridoplasty; congenital adrenal hyperplasia; long-term follow-up; sex assignment; sex of rearing; sexual functioning; vaginoplasty
Year: 2014 PMID: 24400298 PMCID: PMC3877834 DOI: 10.3389/fped.2013.00050
Source DB: PubMed Journal: Front Pediatr ISSN: 2296-2360 Impact factor: 3.418
Current surgical recommendations on feminizing genitoplasty and clitoral surgery.
| The attachment of the clitoris to the pubic arch should not be disrupted |
| Dorsal neurovascular bundles should be preserved. There may be significant lateral branches along the corporal tissue |
| The neurovascular bundles branch distally in a fan fashion toward the glands clitoris |
| Reduction of the clitoral erectile tissue is better achieved with a ventral incision along the urethral plate |
| The urethra and vagina should not be separated |
| Dissection of the bladder from the uterus below the bladder neck should be avoided |
| Using labial and clitoral skin to cover the new introitus is more physiological than rotational skin flaps from the buttocks and perineum |