| A Case of Catel Manzke Syndrome |
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Sang Hyun Oh1, Eun Young Kim1, Young Bong Park1, Sang Kee Park1, Jeong Ryoul Yang2 |
1Departments of Pediatrics, College of Medicine, Chosun University, Kwangju, Korea
2Departments of Plastic Surgery, College of Medicine, Chosun University, Kwangju, Korea |
| Catel Manzke 증후군 1례 |
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오상현1, 김은영1, 박영봉1, 박상기1, 양정열2 |
1조선대학교 의과대학 소아과학교실
2조선대학교 의과대학 성형외과학교실 |
Correspondence:
Sang Hyun Oh, Email: 1
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| Abstract |
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Catel Manzke syndrome is characterized by hyperphalangy of the index fingers associated with Robin malformation sequence. The etiology of Catel Manzke syndrome is still uncertain, with the majority of cases being sporadic. Careful observation to recognize upper airway obstruction secondary to the Robin sequence should be made a part of routine care for newborns with this disorder. Failure to thrive is related to respiratory or cardiac problems. The vast majority of case have normal intelligence. With advancing age, the accessory bone fuses to the proximal phalangeal epiphysis. We report a neonate with the Pierre Robin triad, accessory bone between the second metacarpal and its proximal phalanx of the Rt hand, camptodactyly, coarctation of aorta and hydronephrosis of Lt kidney. |
| Key Words:
Catel Manzke syndrome, Pierre Robin sequence, Hyperphalangy of index finger |
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