Congenital adrenal hyperplasia: Lessons from a multinational study

Hormone Research

Volumn 57, Issue SUPPL. 2, 2002, Pages 95-101

  Frisch, H ^a   Waldhauser, F ^a   Lebl, J ^b   Solyom, J ^c   Hargitai, G ^d   Kovacs, J ^e   Pribilincova, Z ^f   Krzisnik, C ^g   Battelino, T ^h  

^a UNIVERSITY OF VIENNA   (Austria)

^b CHARLES UNIVERSITY   (Czech Republic)

^c SEMMELWEIS UNIVERSITY   (Hungary)

^d EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^e UNIVERSITY OF SZEGED   (Hungary)

^f Children Hospital   (Slovakia)

^g UNIVERSITY CHILDREN S HOSPITAL   (Slovenia)

^h NONE

Author keywords

Body height; Congenital adrenal hyperplasia; Epidemiology; Final height; Genotyping; Growth velocity; Molecular genetics; Mortality; Percentiles

Indexed keywords

ADOLESCENT; ADULT; BODY HEIGHT; CHILD; CONFERENCE PAPER; CONGENITAL ADRENAL HYPERPLASIA; CORRELATION ANALYSIS; EPIDEMIOLOGICAL DATA; FEMALE; GENE MUTATION; GROWTH ACCELERATION; GROWTH RATE; GROWTH RETARDATION; HUMAN; INFANT; INTRON; MAJOR CLINICAL STUDY; MALE; MORTALITY; MUTATION RATE; NEWBORN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PUBERTY; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SALT LOSING NEPHRITIS; SEX DIFFERENCE; SIBLING; AGE; ARTICLE; COHORT ANALYSIS; EUROPE; GENETICS; GROWTH; METHODOLOGY; MUTATION; PATHOPHYSIOLOGY; PRESCHOOL CHILD; RETROSPECTIVE STUDY;

ADOLESCENT; ADRENAL HYPERPLASIA, CONGENITAL; ADULT; AGE FACTORS; BODY HEIGHT; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; EUROPE; FEMALE; GROWTH; HUMAN; INFANT; MALE; MUTATION; POLYMERASE CHAIN REACTION; PUBERTY; RETROSPECTIVE STUDIES; HUMANS;

EID: 0036278968     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000058109     Document Type: Conference Paper

References (11)

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3. Congenital adrenal hyperplasia - A continuum of disorders
4. Mortality in patients with congenital adrenal hyperplasia: A cohort study
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6. A mathematical model for studying the growth of a child
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10. Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): Implications for diagnosis, prognosis and treatment
11. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency