منابع مشابه
Piebaldism and Vitiligo in Two Brothers
Piebaldism is an autosomal dominant uncommon (<1 in 20,000) congenital pigmentary disorder. Depigmented patches are present since birth. They usually remain unchanged throughout life. Vitiligo is its closest differential diagnosis. We report a unique family in which these two dissimilar depigmentations, i.e. piebaldism and vitiligo (with nevus depigmentosus), were noted in two brothers. T...
متن کاملReiter's disease in two brothers.
Reiter's disease affecting more than one member of a family has been reported only rarely. Paronen (1948) described three families in whom several members, including women and children, developed Reiter's disease following dysentery. All other reported cases of familial aggregation of Reiter's disease have concerned males alone and have never occurred as a sequel to dysentery. Trier (1950) and ...
متن کاملThromboangiitis obliterans in two brothers
Two brothers (case 1 and case 2) with erythema nodosum were diagnosed with thromboangiitis obliterans (TAO). The patients were treated with compounds including Danshen Dripping Pills, Fufang Danshen Diwan and Salvia tetramethylpyrazine. The patients were also treated with fibro-blast growth factor to promote epidermal growth and Bayaspirin enteric-coated tablets to reduce platelet aggregation. ...
متن کاملEndomyocardial Fibrosis in Two Brothers.
Endomyocardial fibrosis is a very rare form of heart disease in temperate climates but is fairly common in tropical and sub-tropical parts of Africa. Since Bedford and Konstam (1946) first described the disease in West African soldiers, many reports have appeared from various parts of Africa: from Uganda (Davies, 1948), the Sudan (O'Brien, 1954), Nigeria (Nwokolo, 1955; Abrahams, 1959, 1962), a...
متن کاملAdrenoleukodystrophy: heterogeneity in two brothers.
A man with hypoadrenalism died from a rapidly progressive pseudobulbar palsy, due to adult onset adrenoleukodystrophy. This diagnosis suggested that his brother, with a longstanding spastic paraparesis, suffered from adrenomyeloneuropathy. Both cases were confirmed biochemically. The heterogeneity of expression of this x-linked disorder is described, with the consequent difficulty in diagnosis ...
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ژورنال
عنوان ژورنال: Journal of Nepal Medical Association
سال: 2003
ISSN: 1815-672X,0028-2715
DOI: 10.31729/jnma.1422