کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4289143 1612108 2015 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
A rare case of 3C disease: Ritscher–Schinzel syndrome presenting with recurrent talipes equinovarus
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی عمل جراحی
پیش نمایش صفحه اول مقاله
A rare case of 3C disease: Ritscher–Schinzel syndrome presenting with recurrent talipes equinovarus
چکیده انگلیسی


• Talipes equinovarus can concurrently be seen with several diseases but it can rarely manifest as a component of any syndrome.
• Ritscher–Schinzel syndrome, or cranio-cerebello-cardiac syndrome, is rarely seen and has autosomal recessive inheritance.
• A comprehensive literature review did not show any reports about concurrent hip dysplasia and clubfoot with this Ritscher–Schinzel syndrome.
• So we report this case to raise some awareness that persistent PEV, in some cases, could be a feature of this rare genetical disorder, Ritscher–Schinzel syndrome.

INTRODUCTIONClub foot (CF) is characterized by multiple deformities such as varus, adductus and internal rotation of the forefoot. It is well-known and a frequent congenital disorder. CF can concurrently be seen with several diseases but it can rarely manifest as a component of any other syndrome. Ritscher–Schinzel syndrome, or cranio-cerebello-cardiac syndrome, is rarely seen and has autosomal recessive inheritance. It is characterized by cranio-facial, cerebellar and cardiac abnormalities. We report a case diagnosed as Ritscher–Schinzel syndrome concurrent with persistent CF.PRESENTATION OF CASEA two-year-old boy with persistent CF and concurrent congenital hip dysplasia. Despite successful serial casting and subsequent achilloplasty a clinical relapse was observed in our patient. After a detailed phenotypic evaluation, genetical tests and imaging technique the patient was diagnosed 3C Ritscher–Schinzel syndrome.DISCUSSIONA comprehensive literature review did not show any reports about concurrent hip dysplasia and clubfoot in Ritscher–Schinzel syndrome. We report that CF may be associated with rare genetical abnormalities.CONCLUSIONWith this report we would like to raise awareness about the possible association of persistent CF with this rare genetical disorder, Ritscher–Schinzel syndrome. It should be included in differential diagnosis of patients with persistent CF.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Surgery Case Reports - Volume 7, 2015, Pages 130–133
نویسندگان
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