منابع مشابه
Netherton syndrome: report of two cases
Netherton syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is trichorrhexis invaginata identified by microscopic examination of hair shaft. Ichthyosis linearis circumflexa is ano...
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Deux cas de Syndr'.:lme de Wilson-Mikity sont rapportes: le premier c:mcerne un premature chez qui les signes d'insuffisance re:,piratoire ont debutes tro;s semaines apres !a naissance. La radiographie a mis en evidenc Le deuxieme malade i:-ernit 2.EO::J kilos lors de son hospitalisati::>n a l'ag:c d qu·11,c jous. La radiograp'.1ie pulmonaire mett en ev;dencde:, opacite rec!iculaires bilatera...
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As a culture-bound syndrome, koro is described in the DSM-IV as “an episode of sudden and intense anxiety that the penis (or, in females, the vulva and the nipples) will recede into the body and possibly cause death.” Sometimes the syndrome may occur as an epidemic involving several hundreds to thousands of people within a short period of time. While the syndrome individually involves an anxiet...
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binder’s syndrome is an uncommon entity characterized by midfacial hypoplasia along with class iii incisal relationship. the individuals with this syndrome are easily recognizable and the syndrome is mostly associated with other malocclusions. the current article presents two cases of this rare syndrome and describes its general features. key words: binder’s, midfacial hypoplasia, maxillofacial...
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Two different cases of Stevens - Johnson syndrome are reported. We used intravenous immunoglobulin in their management and compared the results of treatment with the conventional lines of therapy in a historical control.
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ژورنال
عنوان ژورنال: The Japanese Journal of Sarcoidosis and Other Granulomatous Disorders
سال: 2013
ISSN: 1883-1273
DOI: 10.7878/jjsogd.33.91