Clinical and laboratorial features that may differentiate 46,XY DSD due to partial androgen insensitivity and 5 -reductase type 2 deficiency

International Journal of Endocrinology

Volumn 2012, Issue , 2012, Pages

  Veiga, Nélio Neves ^a   Medaets, Pedro Augusto Rodrigues ^a   Petroli, Reginaldo José ^a   Calais, Flávia Leme ^a   De Mello, Maricilda Palandi ^a   De Sousa Castro, Carla Cristina Telles ^a   Guaragna Filho, Guilherme ^a   Sewaybricker, Letícia Espósito ^a   Marques De Faria, Antonia Paula ^a   MacIel Guerra, Andréa Trevas ^a   Guerra, Gil ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROSTANOLONE; ANDROSTENEDIONE; FOLLITROPIN; LUTEINIZING HORMONE; THYROXINE;

5ALPHA REDUCTASE TYPE 2 DEFICIENCY; ADULT; ANDROGEN INSENSITIVITY SYNDROME; AR GENE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BIRTH WEIGHT; BODY HEIGHT; CHILD; DISEASE SEVERITY; FAMILIAL INCIDENCE; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; KARYOTYPE 46,XY; MAJOR CLINICAL STUDY; MUTATOR GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEX DIFFERENTIATION DISORDER; SRD5A2 GENE;

EID: 84855597617     PISSN: 16878337     EISSN: 16878345     Source Type: Journal    
DOI: 10.1155/2012/964876     Document Type: Article

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