11 Beta hydroxylase deficiency: A clinical study about seven cases;Le deficit en 11 beta hydroxylase: Etude clinique a propos de sept observations

Tunisie Medicale

Volumn 84, Issue 2, 2006, Pages 106-113

  Khémirí, Monia ^a   Ridane, Hana ^a   Bou Yahia, Olfa ^a   Matoussi, Nadia ^a   Khaldi, Faouzia ^a  

^a CHILDREN S HOSPITAL   (Tunisia)

Author keywords

11beta hydroxylase; Congenital adrenal hyperplasia; Hypertension; Precocious puberty

Indexed keywords

ANTIHYPERTENSIVE AGENT; GLUCOCORTICOID; STEROID 11BETA MONOOXYGENASE;

AMBIGUITY; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL STUDY; CONGENITAL ADRENAL HYPERPLASIA; CONSANGUINITY; CONTROLLED STUDY; CONVULSION; DISEASE ASSOCIATION; DISEASE SEVERITY; ENZYME DEFICIENCY; EPISTAXIS; FACIAL NERVE PARALYSIS; FEMALE; HETEROSEXUALITY; HORMONE SUBSTITUTION; HUMAN; HYPERTENSION; HYPOKALEMIA; MALE; PRADER WILLI SYNDROME; PRECOCIOUS PUBERTY; PRESCHOOL CHILD; RETE TESTIS; RETROSPECTIVE STUDY; SEX RATIO; SEXUAL DEVELOPMENT; TREATMENT DURATION;

ADRENAL HYPERPLASIA, CONGENITAL; CHILD, PRESCHOOL; CONSANGUINITY; FEMALE; HUMANS; HYPERTENSION; INFANT; INFANT, NEWBORN; MALE; PUBERTY, PRECOCIOUS; RETROSPECTIVE STUDIES;

EID: 33744494295     PISSN: 00414131     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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