Nonclassic 21-hydroxylase deficiency

Fertility and Sterility

Volumn 86, Issue SUPPL. 1, 2006, Pages

  New, Maria I ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

21 hydroxylase deficiency; autosomal recessive disorders; congenital adrenal hyperplasia

Indexed keywords

ACNE; ADOLESCENCE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BODY HEIGHT; CONGENITAL ADRENAL HYPERPLASIA; CYSTIC FIBROSIS; ETHNOLOGY; FEMALE STERILITY; GENE IDENTIFICATION; GENE MUTATION; HAIR LOSS; HIRSUTISM; HUMAN; INFERTILITY; MALE STERILITY; MOLECULAR CLONING; NONCLASSIC 21 HYDROXYLASE DEFICIENCY; PRENATAL PERIOD; PRIORITY JOURNAL; PUBERTY; SHORT STATURE; SICKLE CELL ANEMIA; STEROID 21 MONOOXYGENASE DEFICIENCY; TAY SACHS DISEASE;

ADRENAL HYPERPLASIA, CONGENITAL; FEMALE; GENES, RECESSIVE; HUMANS; INCIDENCE; INFERTILITY; MALE;

EID: 33745210399     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2006.03.005     Document Type: Article

References (8)

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7. Zerah M., Ueshiba H., Wood E., Speiser P.W., Crawford C., McDonald T., et al. Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test. a small sample study. J Clin Endocrinol Metab 70 (1990) 1662-1667
8. New M., Carlson A., Obeid J., Marshall I., Cabrera M., Goseco A., et al. Extensive Personal Experience. prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies. J Clin Endocrinol Metab 86 (2001) 5651-5657