A case of lateral facial clefts with fallot tetralogy, duodenal stenosis and intestinal malrotation: A new multiple congenital anomaly syndrome?

Clinical Dysmorphology

Volumn 8, Issue 1, 1999, Pages 19-21

  Kumar, Dhavendra ^a,b  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^b Centre for Human Genetics   (United States)

Author keywords

Duodenal stenosis; Fallot tetralogy; Intestinal malrotation; Lateral facial clefts

Indexed keywords

ARTICLE; CASE REPORT; CLEFT PALATE; DIFFERENTIAL DIAGNOSIS; DUODENUM STENOSIS; EAR MALFORMATION; FACE MALFORMATION; FALLOT TETRALOGY; FEMALE; HUMAN; INTESTINE MALROTATION; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; DUODENUM; FACE; FEMALE; HUMANS; INFANT, NEWBORN; INTESTINES; SYNDROME; TETRALOGY OF FALLOT;

EID: 0033008067     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

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4. Poswillo D (1973). The pathogenesis of the first and second branchial arch syndromes. Oral Surg 35:301.
5. Robinson LK, Hoyme HE, Edwards DK. (1987). Vascular pathogenesis of unilateral craniofacial defects. J Pediatr 111:236.
6. Winter RM, Baraitser M (1996). London Dysmorphology Database. Oxford Medical Databases. Oxford: Oxford University Press.