Literature DB >> 8469494

Prenatal diagnosis and obstetric management of Larsen syndrome.

B Rochelson1, B Petrikovsky, S Shmoys.   

Abstract

BACKGROUND: Larsen syndrome is a disease of generalized defect in collagen formation including multiple disorders of the joints and cardiac anomalies. A review of the literature revealed no previous reported cases in pregnancy. CASE: A 29-year-old woman with known Larsen syndrome thought to be of the autosomal recessive type presented in pregnancy; second-trimester ultrasound suggested fetal involvement with Larsen syndrome. The patient was followed with serial ultrasounds, and she had pediatric and anesthesiologic consultations. She was delivered by cesarean of a female infant whose neck was immediately stabilized. The infant was then taken to the neonatal intensive care unit, where a diagnosis of Larsen syndrome was confirmed.
CONCLUSIONS: Larsen syndrome, which may be diagnosed prenatally, is a rare and unique condition that requires multidisciplinary care. Obstetric management must take into account the increased anesthetic and surgical risks to the mother and the risk of fetal injury including cervical spine instability. The genetics of Larsen syndrome are also discussed.

Entities:  

Mesh:

Year:  1993        PMID: 8469494

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  5 in total

1.  Antenatal diagnosis of Larsen syndrome.

Authors:  M L Kulkarni; Mohamed Haseen Basha; Sudhakar Hegade; Thiyagaraj A Kumarasamy; Akhil M Kulkarni
Journal:  Indian J Pediatr       Date:  2010-07       Impact factor: 1.967

2.  Larsen syndrome--lethal variety.

Authors:  M L Kulkarni; Zaheeruddin Mohammed; Preethi M Kulkarni
Journal:  Indian J Pediatr       Date:  2005-12       Impact factor: 1.967

3.  A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Authors:  Louise S Bicknell; Claire Farrington-Rock; Yousef Shafeghati; Patrick Rump; Yasemin Alanay; Yves Alembik; Navid Al-Madani; Helen Firth; Mohammad Hassan Karimi-Nejad; Chong Ae Kim; Kathryn Leask; Melissa Maisenbacher; Ellen Moran; John G Pappas; Paolo Prontera; Thomy de Ravel; Jean-Pierre Fryns; Elizabeth Sweeney; Alan Fryer; Sheila Unger; L C Wilson; Ralph S Lachman; David L Rimoin; Daniel H Cohn; Deborah Krakow; Stephen P Robertson
Journal:  J Med Genet       Date:  2006-06-26       Impact factor: 6.318

4.  Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene.

Authors:  N Winer; F Kyndt; A Paumier; A David; B Isidor; M Quentin; B Jouitteau; P Sanyas; H J Philippe; A Hernandez; D Krakow; C Le Caignec
Journal:  Prenat Diagn       Date:  2009-02       Impact factor: 3.050

5.  Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

Authors:  M Vujic; K Hallstensson; J Wahlström; A Lundberg; C Langmaack; T Martinson
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.