Cardiac surgery unmasks latent hypoparathyroidism in a child with the 22q11.2 deletion syndrome

Journal of Pediatric Endocrinology and Metabolism

Volumn 19, Issue 7, 2006, Pages 943-946

  Schaan, Beatriz D'Agord ^a   Huber, Janaina ^a   Leitet, Julio Cesar L ^b   Kiss, Andrea ^c  

^a INSTITUTO DE CARDIOLOGIA DO RIO GRANDE DO SUL   (Brazil)

^b FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

^c Federal Foundation School of Medical Sciences   (Brazil)

Author keywords

Calcium; Congenital; Di George anomaly; Heart defects; Hypoparathyroidism; Tetralogy of Fallot

Indexed keywords

AMIODARONE; CALCITRIOL; CALCIUM; INOTROPIC AGENT; PARATHYROID HORMONE;

ARTICLE; CALCIUM BLOOD LEVEL; CALCIUM METABOLISM; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; DIGEORGE SYNDROME; DISEASE COURSE; DISEASE DURATION; DOSE RESPONSE; FACE DYSMORPHIA; FALLOT TETRALOGY; FEMALE; GENETIC ANALYSIS; GIRL; HEART ARRHYTHMIA; HEART SURGERY; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; INCIDENTAL FINDING; PARATHYROID HORMONE BLOOD LEVEL; POSTOPERATIVE PERIOD; PRESCHOOL CHILD;

EID: 33748445297     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2006.19.7.943     Document Type: Article

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