Familial Bird-headed Dwarfism (Seckel's Syndrome)

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چکیده

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منابع مشابه

Familial dwarfism: case report.

MIDDLEKAMP, J.N. & HAFFNER, H. (1963) Carcinoma of the colon in children. Pediatrics, 32, 558. MORSON, B.C. & BUSSEY, H.J.R. (1970) Predisposing Causes of Intestinal Cancer-(monograph) Chicago, p. 31. Year Book Publishers, Inc. O'BRIEN, S.E. (1967) Carcinoma of the colon in childhood and adolescence. Canadian Medical Association Journal, 96, 1217. STALPORT, J. & LETAWE, P. (1971) Gardner's synd...

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A Case Study of Camptomelic Dwarfism Syndrome

Camptomelic dwarfism or dysplas1a is a rare syndrome in which· short stature is associated with angulation and bowing of the lower limb Long bones, hypoplasia of the facial bones and scapula and various other skeletal and respiratory and nervous system. A 9 day old girl with this syndrome was admitted in our peiatric Department, Loghman Hospital medical center because of Dwarfism and hypotonia....

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3-M Syndrome / Primordial Dwarfism Panel

Numerous monogenic causes of growth disorders have been identified. Inheritance of most disorders covered by this panel is autosomal recessive, but familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome is considered to have autosomal dominant inheritance. This panel covers, but is not limited to, genes and disorders covered by the subpanels. and therefore enables ef...

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3-M Syndrome / Primordial Dwarfism Panel

Numerous monogenic causes of growth disorders have been identified. Inheritance of most disorders covered by this panel is autosomal recessive, but familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome is considered to have autosomal dominant inheritance. This panel covers, but is not limited to, genes and disorders covered by the subpanels. and therefore enables ef...

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3-M Syndrome / Primordial Dwarfism Panel

Numerous monogenic causes of growth disorders have been identified. Inheritance of most disorders covered by this panel is autosomal recessive, but familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome is considered to have autosomal dominant inheritance. This panel covers, but is not limited to, genes and disorders covered by the subpanels. and therefore enables ef...

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ژورنال

عنوان ژورنال: Journal of Medical Genetics

سال: 1973

ISSN: 1468-6244

DOI: 10.1136/jmg.10.2.196