Literature DB >> 269694

Werner syndrome.

S K Samantray, S Samantray, S C Johnson, A Bhaktaviziam.   

Abstract

A case of Werner syndrome is reported. The patient was prematurely old, had skin atrophy, characteristic posterior subcapsular cataracts and prepubertal primary hypogonadism. Additional ocular features compatible with premature ageing included presbyopia, arcus seniles and diminished tear flow. Diabetes mellitus, poliosis, baldness and beak-like nose were not present.

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Year:  1977        PMID: 269694     DOI: 10.1111/j.1445-5994.1977.tb03695.x

Source DB:  PubMed          Journal:  Aust N Z J Med        ISSN: 0004-8291


  1 in total

1.  Quantitative assessment of craniofacial morphology in Johanson-Blizzard syndrome.

Authors:  Curtis K Deutsch; Tania Hreczko; Lewis B Holmes
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2013-03-06
  1 in total

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