Familial Poland anomaly.
نویسنده
چکیده
The Poland anomaly is usually a non-genetic malformation syndrome. This paper reports two second cousins who both had a typical left sided Poland anomaly, and this constitutes the first recorded case of this condition affecting more than one member of a family. Despite this, for the purposes of genetic counselling, the Poland anomaly can be regarded as a sporadic condition with an extremely low recurrence risk.
منابع مشابه
Debendox does not cause the Poland anomaly.
The suggestion that Debendox may cause the Poland anomaly is refuted by a study of the antenatal drug exposure in 46 cases of the Poland anomaly and 32 cases of isolated absence of the pectoralis major. Debendox had been prescribed in one case of the Poland anomaly and in one case of isolated pectoralis absence, but in neither was the compound given during organogenesis. In none of the 78 cases...
متن کاملPoland anomaly with dextrocardia: a case report.
Poland anomaly was first reported in Guys Hospital report, 1841. Since then many cases have been described. Among the upper limb developmental defects, Poiand anomaly has a prevalence of 1 in 20,000. According to anotherreport 10% of all cases of upper limb syndactyly have Poland anomaly also. Poland anomaly is a sporadic developmental disorder involving the upper limb. Primary defect seems to ...
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We report an atypical case of the Poland anomaly. Unreported features are that the hand abnormality is on the contralateral side to the chest wall defect, there is an ulnar ray predominance, and lack of syndactyly.
متن کاملPoland syndrome with dextrocardia and congenital heart disease: A case report
The Poland syndrome is a rare anomaly. It consists of unilateral absence or hypoplasia of the pectoralis muscle, most frequently involving the sternocostal portion and a variable degree of ipsilateral hand and digit anomalies. The combination of Poland syndrome and dextrocardia is uncommon. We describe a case of Poland syndrome with dextrocardia and Patent ductus arteriosus.
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ورودعنوان ژورنال:
- Journal of medical genetics
دوره 19 4 شماره
صفحات -
تاریخ انتشار 1982