منابع مشابه
A Case of Macrodactyly
S., a Hindu girl, aged 10 years, of the village Saraiyan, in Ghazipnr district, was admitted into the hospital with abnormal enlargement of the right middle finger. She came to the hospital for its removal, as she had been feeling its weight. It is seven and a half inches in length and seven and a half inches in diameter at its thickest part. The left middle finger is three inches in length and...
متن کاملMacrodactyly.
We report the results of the treatment of 23 patients with macrodactyly. Eighteen had a two-stage bulk-reducing (defatting) procedure; phalangectomy was used to shorten the digits. At a mean follow-up of nine years (2 to 12), two patients had been lost to follow-up, and three await a second-stage procedure. Good cosmetic correction was achieved in 12 patients, with satisfactory results in seven...
متن کاملCongenital macrodactyly: a clinical study.
Congenital macrodactyly is a rare congenital malformation characterised by progressive enlargement of all mesenchymal elements of a digit. The present study is an attempt to draw the attention towards the similarities and differences between macrodactyly of the hand and foot. Radiographical, operative findings and histopathological examination of five cases are included in the present study. Em...
متن کاملA case of disproportionate macrodactyly or a mild form of Proteus syndrome? An interesting case.
We present a 20-year-old Malay male whom we believe has Proteus syndrome, a rare congenital disorder of asymmetrical overgrowth of body tissues. There are fewer than 100 confirmed cases reported worldwide thus the clinical presentation and histopathological findings are of significance. Our patient presented with an overgrown right small finger and subcutaneous purplish pigmentation over his le...
متن کاملASTERNIA: A CASE REPORT
Absence of the sternum or asterniais the rarest developmental anomaly of the stern um. A female newborn is presented with asternia and ASD.
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ژورنال
عنوان ژورنال: National Journal of Clinical Anatomy
سال: 2012
ISSN: 2277-4025
DOI: 10.4103/2277-4025.297944