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Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesis.
Eur J Pediatr ; 122(1): 1-17, 1976 Apr 06.
Article en En | MEDLINE | ID: mdl-1261565
ABSTRACT
Two infants with the Hanhart syndrome, i.e. micrognathia, microglossia, terminal deficiency of all limbs and imperforate anus in one, were dissected and studied in detail. The interrelationships of the muscular and skeletal defects suggested that they were the result of incomplete rather than abnormal morphogenesis. We speculate that the oral and limb abnormalities resulted from deficient mesodermal proliferation caused by disturbances in the ectodermal-mesodermal interactions beginning about the 4th week of development. The imperforate anus may also relate to the proposed defect.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ectromelia / Disostosis Mandibulofacial Tipo de estudio: Etiology_studies Límite: Humans / Newborn Idioma: En Revista: Eur J Pediatr Año: 1976 Tipo del documento: Article
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ectromelia / Disostosis Mandibulofacial Tipo de estudio: Etiology_studies Límite: Humans / Newborn Idioma: En Revista: Eur J Pediatr Año: 1976 Tipo del documento: Article