منابع مشابه
Congenital Hemangiopericytoma: A Case Report
Hemangiopericytoma is a rare vascular tumor observed mostly in adults. It usually presents with a painless slowly enlarging mass. The infantile type with much rarer occurrence has a different course compared to adults. Very few case reports have been described in the literature with disease onset in the infancy. The first reported case of infantile hemangiopericytoma of limbs from the Middle ...
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We report a twenty-seven-year-old man with the absence of hair on the scalp and eyebrows, which began shortly after his birth. One of his brothers had this problem too. Considering clinical signs and skin biopsy report of the patient, a diagnosis of congenital atrichia was made. The latest findings on the genetic of this disease will be reviewed.
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The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dysplasia is death bearing which is derived from Greek word. It occurs 1in 20,000 to 50,000. It is mainly due to mutations in the fibroblast growth factor receptor 3gene. Features of thanatophoric dysplasia are frontal bossing, prominent eyes, narrow thorax, protruded abdomen and bowed legs. The knowle...
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ژورنال
عنوان ژورنال: Nippon Jibiinkoka Gakkai Kaiho
سال: 2004
ISSN: 0030-6622,1883-0854
DOI: 10.3950/jibiinkoka.107.665