Sonography in prenatal diagnosis of congenital adrenal hyperplasia

Prenatal Diagnosis

Volumn 24, Issue 8, 2004, Pages 627-630

  Saada, Julien ^a,b   Grebille, Anne Gaëlle ^a   Aubry, Marie Cécile ^a   Rafii, Arash ^a   Dumez, Yves ^a   Benachi, Alexandra ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b Paul Sabatier University   (France)

Author keywords

Congenital adrenal hyperplasia; Ultrasound

Indexed keywords

ALDOSTERONE; STEROID 21 MONOOXYGENASE;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CONGENITAL ADRENAL HYPERPLASIA; DISEASE SEVERITY; FAMILY HISTORY; FEMALE; FETUS; FETUS ECHOGRAPHY; FIRST TRIMESTER PREGNANCY; GENE MUTATION; HUMAN; INCIDENCE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SECOND TRIMESTER PREGNANCY; STEROID 21 MONOOXYGENASE DEFICIENCY; VIRILIZATION; WASTING SYNDROME;

ADRENAL GLANDS; ADRENAL HYPERPLASIA, CONGENITAL; ADULT; CHORIONIC VILLI SAMPLING; DEXAMETHASONE; FEMALE; GENITALIA; GESTATIONAL AGE; GLUCOCORTICOIDS; HUMANS; KARYOTYPING; MALE; PREGNANCY; PSEUDOHERMAPHRODITISM; STEROID 21-HYDROXYLASE; ULTRASONOGRAPHY, PRENATAL;

EID: 4243166996     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.948     Document Type: Article

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