Head and neck manifestations of 22q11.2 deletion syndromes

European Archives of Oto-Rhino-Laryngology

Volumn 269, Issue 2, 2012, Pages 381-387

  Marom, Tal ^a   Roth, Yehudah ^a,b   Goldfarb, Abraham ^a   Cinamon, Udi ^a  

^a TEL AVIV UNIVERSITY   (Israel)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

Development; DiGeorge syndrome; Malformation; Thyroid disease

Indexed keywords

IMMUNOGLOBULIN E; PARATHYROID HORMONE; THYROTROPIN;

ADULT; ASPIRATION BIOPSY; CAROTID ARTERY ANOMALY; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 22Q11; CHROMOSOME LOSS; CLEFT PALATE; CLINICAL FEATURE; COMPUTED TOMOGRAPHIC ANGIOGRAPHY; DISEASE ASSOCIATION; ECHOGRAPHY; EOSINOPHIL; EOSINOPHILIA; ESOPHAGUS MALFORMATION; FECES CULTURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GOITER; GRAVES DISEASE; HEAD AND NECK MALFORMATION; HUMAN; HYPOCALCEMIA; HYPOPARATHYROIDISM; HYPOTHYROIDISM; LARYNGOSCOPY; LARYNX DISORDER; MALE; MEDICAL HISTORY; MEDICAL LITERATURE; MENTAL PATIENT; NAUSEA; PARATHYROID GLAND; PRIORITY JOURNAL; REVIEW; THYMUS APLASIA; THYROID ADENOMA; THYROID CANCER; THYROID GLAND; THYROIDECTOMY; TRACHEA DISEASE; UPPER GASTROINTESTINAL BLEEDING; VOMITING;

22Q11 DELETION SYNDROME; ADENOMA; ADULT; ARTERIOVENOUS MALFORMATIONS; CAROTID ARTERIES; CERVICAL VERTEBRAE; CHILD, PRESCHOOL; CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DNA-BINDING PROTEINS; FEMALE; GENE KNOCKOUT TECHNIQUES; GENES, SUPPRESSOR; HUMANS; IMAGE INTERPRETATION, COMPUTER-ASSISTED; IMAGING, THREE-DIMENSIONAL; LOSS OF HETEROZYGOSITY; MALE; OTORHINOLARYNGOLOGIC DISEASES; RESPIRATORY SYSTEM ABNORMALITIES; SKULL BASE; THYROID NEOPLASMS; TOMOGRAPHY, X-RAY COMPUTED; TRANSCRIPTION FACTORS; YOUNG ADULT;

EID: 84857063064     PISSN: 09374477     EISSN: 14344726     Source Type: Journal    
DOI: 10.1007/s00405-011-1745-1     Document Type: Review

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