Punctate epiphyses associated with Turner syndrome

Pediatric Radiology

Volumn 29, Issue 6, 1999, Pages 478-480

  Morrison, Stuart C ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CALCIFYING CHONDRODYSTROPHY; CASE REPORT; CHONDRODYSPLASIA PUNCTATA; CHROMOSOME DELETION X; EPIPHYSIS; FETUS; HUMAN; PRIORITY JOURNAL; SEX CHROMOSOME ABERRATION; TURNER SYNDROME;

ADULT; CHONDRODYSPLASIA PUNCTATA; EPIPHYSES; FEMALE; FETAL DISEASES; HUMANS; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; TURNER SYNDROME; X CHROMOSOME;

EID: 0033058340     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470050622     Document Type: Article

References (6)

1. Camera G, Mastroiacovo P (1982) Birth prevalence of skeletal dysplasias in the Italian multicentric monitoring system for birth defects. In: Papadatos CJ, Bartsocas CE (eds) Skeletal dysplasias, Liss, New York, pp 441-449
2. Poznanski AK (1994) Punctate epiphyses: a radiological sign not a disease. Pediatr Radiol 24: 418-424
3. Bartoletti S, Armfield SL III, Ledesma-Medina J (1978) The cerebro-hepato-renal (Zellweger's) syndrome: report of four cases. Radiology 127: 741-745
4. Curry CJR, Magenis RE, Brown M, et al (1984) Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome. N Engl J Med 311: 1008-1015
5. Wulfsherg EA, Curtis J, Jayne CH (1992) Chondrodysplasia punctata: a boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders. Am J Med Genet 43: 823-828
6. Kurtz AB, Filly RA, Wapner RJ, et al (1986) In utero analysis of heterozygous achondroplasia: variable time of onset as detected by femur length measurements. J Ultrasound Med 5: 137-140