Multiple neural fibrolipomas with macrodactyly
نویسندگان
چکیده
منابع مشابه
Macrodactyly.
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 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 کاملExpression Analysis of Macrodactyly Identifies Pleiotrophin Upregulation
Macrodactyly is a rare family of congenital disorders characterized by the diffuse enlargement of 1 or more digits. Multiple tissue types within the affected digits are involved, but skeletal patterning and gross morphological features are preserved. Not all tissues are equally involved and there is marked heterogeneity with respect to clinical phenotype. The molecular mechanisms responsible fo...
متن کاملMacrodactyly, Hemihyperplasia, and the Dysmorphic First Ray
Congenital overgrowth disorders of the lower extremity have been rarely reported in podiatric literature. Since the 1980s, however, advancements in genetics and diagnostic imaging have allowed for a better understanding of these conditions. The etiologies of overgrowth conditions are largely unknown. Although overgrowth conditions are highly variable, clinically, these patients present similarl...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology
سال: 2011
ISSN: 0019-5154
DOI: 10.4103/0019-5154.91851