Literature DB >> 3517360

In utero analysis of heterozygous achondroplasia: variable time of onset as detected by femur length measurements.

A B Kurtz, R A Filly, R J Wapner, M S Golbus, M R Rifkin, P W Callen, M E Pasto.   

Abstract

Seven cases of heterozygous achondroplasia were examined in utero. Although the head shape and growth were normal, the initially normal femur length showed a decrease in growth and fell below the lower 99 per cent confidence limit in all cases. The time of presentation of achondroplasia varied between 21 and 27 gestational weeks. This study suggests that the diagnosis of achondroplasia can be reasonably made when the femur is abnormally short. When the femoral length is appropriate prior to 30 weeks, more caution should be taken in interpretation. Because of the variability in presentation, the fetus could be normal or still could be affected.

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Year:  1986        PMID: 3517360     DOI: 10.7863/jum.1986.5.3.137

Source DB:  PubMed          Journal:  J Ultrasound Med        ISSN: 0278-4297            Impact factor:   2.153


  4 in total

Review 1.  The weight of the fourth dimension for the diagnosis of genetic bone disease.

Authors:  A Giedion
Journal:  Pediatr Radiol       Date:  1994

2.  Fetal imaging in the skeletal dysplasias: overview and experience.

Authors:  R S Lachman
Journal:  Pediatr Radiol       Date:  1994

Review 3.  Achondroplasia: a comprehensive clinical review.

Authors:  Richard M Pauli
Journal:  Orphanet J Rare Dis       Date:  2019-01-03       Impact factor: 4.123

4.  SHOX haploinsufficiency presenting with isolated short long bones in the second and third trimester.

Authors:  Shwetha Ramachandrappa; Abhijit Kulkarni; Hina Gandhi; Cheryl Ellis; Renata Hutt; Lesley Roberts; Rosol Hamid; Aris Papageorghiou; Sahar Mansour
Journal:  Eur J Hum Genet       Date:  2018-01-12       Impact factor: 4.246

  4 in total

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