Abstract
Abstract An autopsy case of Klippel‐Feil syndrome with the classical triad of short neck, low posterior hairline and limitation of neck movement is reported. The patient died of cardiac failure resulting from complicated serious cardiovascular anomalies such as double outlet right ventricle, congenital mitral valve stenosis and coarctation of aorta. The condition was also complicated by radial ray deficiency of the left arm and asymmetry of the thyroid gland. Narrowing of the left subclavian and axillary arteries was detected by angiography while the patient was alive, a finding which may suggest the etiology of this congenital anomaly complex.
Original language | English (US) |
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Pages (from-to) | 107-114 |
Number of pages | 8 |
Journal | Congenital Anomalies |
Volume | 31 |
Issue number | 3 |
DOIs | |
State | Published - Sep 1991 |
Externally published | Yes |
Keywords
- Klippel‐Feil syndrome
- complications
- congenital heart anomaly
- pathogenesis
- upper limb anomaly
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Embryology
- Developmental Biology