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 کاملHypertelorism correction: what happens with growth? Evaluation of a series of 95 surgical cases.
BACKGROUND This report documents the authors' experience with 95 hypertelorism corrections performed since 1971. The authors note their findings regarding outcomes, preferred age at surgery, technique, and stability of results with growth. METHODS Patients were classified into three groups: midline clefts (with or without nasal anomalies, Tessier 0 to 14); paramedian clefts (symmetric or asym...
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: Proceedings of the Royal Society of Medicine
سال: 1927
ISSN: 0035-9157
DOI: 10.1177/003591572702000411