Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Journal of Pediatric Endocrinology and Metabolism

Volumn 18, Issue 2, 2005, Pages 133-142

  Motaghedi, R ^a   Betensky, B P ^a,b   Slowinska, B ^a   Cerame, B ^a   Cabrera, M ^a,c   New, Maria I ^a,b   Wilson, R C ^a,b  

^a Department of Obstetrics Gynecology   (United States)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^c Children's Hospital of Omaha   (United States)

Author keywords

11 hydroxylase deficiency; Congenital adrenal hyperplasia; Prenatal diagnosis; Virilization

Indexed keywords

COMPLEMENTARY DNA; DEXAMETHASONE; STEROID 11BETA MONOOXYGENASE;

AMNIOCENTESIS; ARTICLE; CHROMOSOME MAP; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; DISEASE CARRIER; DNA DETERMINATION; ENZYME DEFICIENCY; EXON; FEMALE; FETUS; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; HOMOZYGOSITY; HUMAN; KARYOTYPING; LINKAGE ANALYSIS; MALE; MOTHER FETUS RELATIONSHIP; MUTATION RATE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PRENATAL DIAGNOSIS; PRENATAL DRUG EXPOSURE; PRENATAL PERIOD; PRENATAL SCREENING; VIRILIZATION;

EID: 14544272897     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2005.18.2.133     Document Type: Article

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