Article
Successful Live Birth in a Woman With 17α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer.
The Journal of clinical endocrinology and metabolism - 1 Feb 2016
Bianchi Paulo Homem de Mello, Gouveia Gabriela Romanenghi Fanti Carvalho Araujo, Costa Elaine M Frade, Domenice Sorahia, Martin Regina M, de Carvalho Luciane Carneiro, Pelaes Tatiana, Inacio Marlene, Codarin Rodrigo Rocha, Sator de Faria Maria Beatriz, Francisco Rossana Pulcineli Vieira, Baracat Edmund Chada, Serafini Paulo César, Mendonca Berenice B
Abstract excerpt
CONTEXT: Congenital adrenal hyperplasia (CAH) due to 17α-hydroxylase deficiency in 46,XX patients is characterized by primary amenorrhea, absent or incomplete sexual maturation, infertility, low serum levels of estradiol, and elevated progesterone (P). There were no previous reports of singleton live births from such women. OBJECTIVE: To describe the first successful singleton live birth in a female with CAH due...
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