1220 THANATOPHORIC DWARFISM AND THE CLOVERLEAF SKULL

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منابع مشابه

Cloverleaf Skull and Thanatophoric Dwarfism

Partington, M. W., Gonzales-Crussi, F., Khakee, S. G., and Wollin, D. G. (1971). Archives of Disease in Childhood, 46, 656. Cloverleaf skull and thanatophoric dwarfism: report of four cases, two in the same sibship. Four cases of the cloverleaf skull syndrome are reported, 3 from Britain and 1 from Canada in a family of German/Irish descent. All cases had generalized chondrodysplastic changes a...

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Cloverleaf skull and thanatophoric dwarfism. Report of four cases, two in the same sibship.

Partington, M. W., Gonzales-Crussi, F., Khakee, S. G., and Wollin, D. G. (1971). Archives of Disease in Childhood, 46, 656. Cloverleaf skull and thanatophoric dwarfism: report of four cases, two in the same sibship. Four cases of the cloverleaf skull syndrome are reported, 3 from Britain and 1 from Canada in a family of German/Irish descent. All cases had generalized chondrodysplastic changes a...

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Thanatophoric dwarfism.

A review of the radiographs of children previously classified as achondroplasiacs revealed six thanatophoric dwarfs. The main radiological differentiating features were the greater degree of shortening of the long bones, including the fibula, the curvature of the femora, the very small size of the thorax and, particularly, the very narrow ossified elements of the vertebral bodies. Perhaps the m...

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Diagnosis of thanatophoric dwarfism in utero.

A 29-year-old multipara presented at the University Hospital, Kuala Lumpur at 26 weeks gestation. She has had two normal deliveries at this hospital, a girl in 1977 and a boy in 1978. Both children are normal and healthy. In this third pregnancy uterine size was larger than dates and hydramnios was suspected. Sonography confirmed the hydramnios and showed a single foetus with hydrocephalus and ...

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Cloverleaf skull syndrome: case report*

The present report is aimed at describing a rare case of cranial malformation - cloverleaf skull syndrome -, whose presence was noticed after the birth of a child with signs of abnormality. Imaging diagnosis methods such as computed tomography and conventional radiography were used to characterize the syndrome.

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ژورنال

عنوان ژورنال: Pediatric Research

سال: 1981

ISSN: 0031-3998,1530-0447

DOI: 10.1203/00006450-198104001-01246