Variant Carvajal syndrome with additional dental anomalies

被引:9
作者
Barber, Sophy [1 ]
Day, Peter [2 ]
Judge, Mary [3 ]
O' Toole, Edell [4 ]
Fayle, Stephen [2 ]
机构
[1] Leeds Dent Inst, Dept Orthodont, Leeds LS2 9LU, W Yorkshire, England
[2] Leeds Dent Inst, Dept Paediat Dent, Leeds LS2 9LU, W Yorkshire, England
[3] Salford Royal NHS Fdn Trust, Dept Dermatol, Salford, Lancs, England
[4] Univ London, Dept Dermatol, London, England
关键词
WOOLLY HAIR; PALMOPLANTAR KERATODERMA; CARDIAC ABNORMALITIES; NAXOS-DISEASE; DESMOPLAKIN; CARDIOMYOPATHY; MUTATIONS; SKIN; FAMILY;
D O I
10.1111/j.1365-263X.2012.01230.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
International Journal of Paediatric Dentistry 2012; 22: 390396 Background This paper aims to review the case of a girl who presented with a number of dental anomalies, in addition to unusual skin, nail and hair conditions. Tragically an undiagnosed cardiomyopathy caused unexpected sudden death. The case is discussed with reference to a number of dermatological and oral conditions which were considered as possible diagnoses. Case Report AW had been under long term dental care for prepubertal periodontitis, premature root resorption of primary teeth, soft tissue and dental anomalies, and angular cheilitis. Separately she had also been seen by several dermatologists with respect to palmar plantar keratosis, striae keratoderma, wiry hair and abnormal finger nails. Tragically the patient suffered a sudden unexpected death and the subsequent post mortem identified an undiagnosed dilated cardiomyopathy. Conclusion The most likely diagnosis is that this case is a variant of Carvajal Syndrome with additional dental anomalies. To date we have been unable to identify mutations in the desoplakin gene. We aim to emphasise the importance of recognising these dental and dermatological signs when they present together as a potential risk factor for cardiac abnormalities.
引用
收藏
页码:390 / 396
页数:7
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