Fraser syndrome in a 96-year-old female

Age and Ageing

Volumn 35, Issue 6, 2006, Pages 642-643

  Impallomeni, Mario ^a   Subramanian, Deepak ^b   Mahmood, Nazim ^b   Joseph, Illes ^c  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b SELLY OAK HOSPITAL   (United Kingdom)

^c DORSET COUNTY HOSPITAL   (United Kingdom)

Author keywords

Cryptophthalmos; Elderly; Fraser syndrome; Syndactyly

Indexed keywords

CIPROFLOXACIN;

AGED; ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE DISORDER; BONE MALFORMATION; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; CLINICAL EXAMINATION; CLINICAL FEATURE; EAR MALFORMATION; EYE MALFORMATION; FEMALE; FRASER SYNDROME; HUMAN; LABORATORY TEST; LARYNX STENOSIS; LIFE EXPECTANCY; LIVER DISEASE; LUNG MALFORMATION; NOSE MALFORMATION; PRIORITY JOURNAL; SYNDACTYLY; URINARY TRACT INFECTION; UROGENITAL TRACT MALFORMATION;

AGE FACTORS; AGED, 80 AND OVER; FACE; FEMALE; FRASIER SYNDROME; HUMANS;

EID: 33750285716     PISSN: 00020729     EISSN: 14682834     Source Type: Journal    
DOI: 10.1093/ageing/afl109     Document Type: Article

References (3)

1. Fraser GR. Our genetic load: A review of some aspects of genetical variation. Ann Hum Genet 1962; 25: 387-415.
2. Thomas IT, Frias JL, Felix V et al. Isolated and syndromic cryptophthalmos. Am J Med Genet 1986; 25: 85-98.
3. Slavotinek AM, Tifft CJ. Fraser syndrome and cryptophthalmos: Review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes. J Med Genet 2002; 39: 623-33.