منابع مشابه
A report of two cases of pyknodysostosis in two children
pyknodysostosis is a rare bone disease characterzed with short stature,wide fontaneles,small chin,hyperdensity of bones,erosion of tufts of the disatl phalanges,and narrowing of the mandibular angle. pyknodysostosis is inheritted as an autosomal recessive disease and may be seen in both sexes at any age.the patients have normal life span.short stature and bone fractures are their major problems...
متن کاملPretibial Epidermolysis Bullosa: Report of two cases
Pretibial epidermolysis bullosa is a rare variant of hereditary epidermolysis bullosa characterized by the delayed onset of lesions and their localization. We present two cases, a 35-year-old woman and a 21-year-old man. They clinically had pruritus, nodular prurigo-like or lichenified lesions, violaceous scarring, milia, nail dystrophy and in one case albopapuloid lesions on the trunk. Physica...
متن کاملGlutathione transferase activity and formation of macromolecular adducts in two cases of acute methyl bromide poisoning.
OBJECTIVES To determine the activity of glutathione transferase and to measure the S-methylcysteine adducts in blood proteins, after acute inhalation exposure to methyl bromide. To examine the influence of the polymorphism of glutathione-S-transferase theta (GSTT1) on the neurotoxicity of methyl bromide. METHODS Two workers acutely exposed to methyl bromide with inadequate respiratory protect...
متن کاملGemistocytic Glioblastomas: Review of Two Cases
We report two cases of de novo Gemistocytic glioblastomas. In case one, a 35 year male presented with features of raised intracranial pressure and rapid neurological deterioration. In case 2; a 73 year old male presented with rapid neurological deterioration and focal neurological deficits. In both cases imaging findings were suggestive of high grade malignancy involving the brain. This was ...
متن کاملAngioimmunoblastic Lymphadenopathand Report of Two Rare Cases
Angioimmunoblastic Lymphadenopathy (AIL) is an uncommon disorder which begins with constitutional symptoms. The majority of the patients .has generalized l?7111ph adenopathy, , hepatosplenomegaly and about 40% show cutaneous manifestations such as maculopapular eruption, purpura, urticaria or erythroderma. HisthopathoIogy of lymphnodes has a characteristic picture. The etiology of AIL is unk...
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ژورنال
عنوان ژورنال: Okayama Igakkai Zasshi (Journal of Okayama Medical Association)
سال: 1987
ISSN: 0030-1558,1882-4528
DOI: 10.4044/joma1947.99.1-2_49