5α steroid reductase deficiency in Turkey

Pediatric Endocrinology Reviews

Volumn 3, Issue SUPPL. 3, 2006, Pages 462-469

  Adiyaman, Pelin Bilir ^a,c   Öcal, Gonul ^a   Çetinkaya, Ergun ^a   Akar, Nejat ^a   Uysal, Ali ^a   Duman, Turker ^a   Evliyaoǧlu, Olcay ^a   Aycan, Zehra ^a   Lumbroso, Serge ^b   Sultan, Charles ^b   Berberoǧlu, Merih ^b  

^a ANKARA UNIVERSITY   (Turkey)

^b INSERM   (France)

^c NONE   (Turkey)

Author keywords

5 steroid reductase 2 gene mutation; Homozygote female carriers; Male Pseudohermaphroditism

Indexed keywords

5ALPHA STEROID REDUCTASE 2; ANDROSTANOLONE; STEROID 5ALPHA REDUCTASE; TESTOSTERONE; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; ENZYME DEFICIENCY; EXON; FEMALE; FOLLOW UP; GENE DELETION; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HORMONE DETERMINATION; HUMAN; KARYOTYPE 46,XY; MALE; MALE PSEUDOHERMAPHRODITISM; SCHOOL CHILD; TURKEY (REPUBLIC);

3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE; ADOLESCENT; CHILD; DISORDERS OF SEX DEVELOPMENT; DNA MUTATIONAL ANALYSIS; FEMALE; GENITALIA; HUMANS; INFANT; INFANT, NEWBORN; MALE; PEDIGREE; TURKEY;

EID: 33751018262     PISSN: 15654753     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (28)

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