Literature DB >> 982315

Trisomy 18 and cyclopia.

A F Lang, F M Schlager, H A Gardner.   

Abstract

A stillborn male infant with cyclopia, holoprosencephaly, extracephalic malformations, and trisomy 18 is described. The importance of chromosome studies in infants with severe congenital malformations is discussed.

Entities:  

Mesh：

Year:  1976        PMID： 982315     DOI： 10.1002/tera.1420140210

Source DB:  PubMed          Journal:  Teratology        ISSN： 0040-3709


  5 in total

1.  The human brain and face: mechanisms of cranial, neurological and facial development revealed through malformations of holoprosencephaly, cyclopia and aberrations in chromosome 18.

Authors:  Marjorie C Gondré-Lewis; Temitayo Gboluaje; Shaina N Reid; Stephen Lin; Paul Wang; William Green; Rui Diogo; Marie N Fidélia-Lambert; Mary M Herman
Journal:  J Anat       Date:  2015-09       Impact factor: 2.610

2.  A case of suspected teratogenic holoprosencephaly.

Authors:  M Stabile; A Bianco; S Iannuzzi; M C Buonocore; V Ventruto
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

3.  Descriptive neuropathology of chromosomal disorders in man.

Authors:  F Gullotta; H Rehder; A Gropp
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Chromosomal abnormalities associated with cyclopia and synophthalmia.

Authors:  R O Howard
Journal:  Trans Am Ophthalmol Soc       Date:  1977

5.  Cebocephaly in an infant with trisomy 18.

Authors:  A G Hunter; M Ray; C Langston
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318
  5 in total

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