Literature DB >> 18057679

Spectrum of severe skeletal dysplasias in North India.

Ratna D Puri1, Seema Thakur, I C Verma.   

Abstract

OBJECTIVE: Severe skeletal dysplasias are a group of bone growth disorders characterized by a lethal outcome in utero or infancy. We describe our experience of the severe skeletal dysplasias diagnosed amongst fetal autopsies done at a tertiary level centre over a five year period.
METHODS: We evaluated 15 cases with short limbed dwarfism, of which 13 fetuses were examined after termination of pregnancy and two were evaluated postnatally.
RESULTS: Short rib dysplasia syndromes with or without polydactyly, osteogenesis imperfecta type II, thanatophoric dysplasia, campomelic dysplasia, chondrodysplasia punctata, rhizomelic type and achondrogenesis were the lethal skeletal dysplasias diagnosed.
CONCLUSION: Precise identification of the tye of skeletal dysplasia is paramount for proper genetic counseling. Postnatal examination and detailed radiographic examination of the fetus especially of the pelvis, limbs, skull and spine are essential to identify the type of skeletal dysplasia.

Entities:  

Mesh:

Year:  2007        PMID: 18057679     DOI: 10.1007/s12098-007-0183-y

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  14 in total

1.  Short rib polydactyly syndrome type I (Saldino-Noonan syndrome).

Authors:  Anoop Verma
Journal:  Indian Pediatr       Date:  2005-04       Impact factor: 1.411

2.  Prevalence of lethal osteochondrodysplasias in Denmark.

Authors:  P E Andersen
Journal:  Am J Med Genet       Date:  1989-04

3.  Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosis.

Authors:  S A Rasmussen; F R Bieber; B R Benacerraf; R S Lachman; D L Rimoin; L B Holmes
Journal:  Am J Med Genet       Date:  1996-01-02

4.  Short rib (polydactyly) syndrome type IV: Beemer-Langer syndrome.

Authors:  A K Sharma; S R Phadke; S S Agarwal
Journal:  Am J Med Genet       Date:  1993-05-15

5.  Short rib polydactyly syndrome-Type I.

Authors:  S Sridhar; Ravi Kishore; Niranjan Thomas; Atanu Kumar Jana
Journal:  Indian J Pediatr       Date:  2004-04       Impact factor: 1.967

6.  Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant.

Authors:  J M Connor; R A Connor; E M Sweet; A A Gibson; W J Patrick; M B McNay; D H Redford
Journal:  Am J Med Genet       Date:  1985-10

7.  Suspected skeletal dysplasias: femur length to abdominal circumference ratio can be used in ultrasonographic prediction of fetal outcome.

Authors:  A Rahemtullah; B McGillivray; R D Wilson
Journal:  Am J Obstet Gynecol       Date:  1997-10       Impact factor: 8.661

8.  Prenatal diagnosis of the skeletal dysplasias.

Authors:  R Sharony; C Browne; R S Lachman; D L Rimoin
Journal:  Am J Obstet Gynecol       Date:  1993-09       Impact factor: 8.661

9.  Contribution of three-dimensional computed tomography in the assessment of fetal skeletal dysplasia.

Authors:  M Cassart; A Massez; T Cos; L Tecco; D Thomas; N Van Regemorter; F Avni
Journal:  Ultrasound Obstet Gynecol       Date:  2007-05       Impact factor: 7.299

10.  Antenatal detection of skeletal dysplasias.

Authors:  Barbara V Parilla; Elizabeth A Leeth; Michelle P Kambich; Patricia Chilis; Scott N MacGregor
Journal:  J Ultrasound Med       Date:  2003-03       Impact factor: 2.153

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  4 in total

1.  Prenatal third trimester sonographic behavior of a thanatophoric dwarfs.

Authors:  Adekunle Y Abdulkadir; Kabiru Isyaku; Akintade Dare; Sulaiman G Abdullahi; Sule K Idris; Abdulkadir M Tabari
Journal:  J Prenat Med       Date:  2008-10

Review 2.  A review of skeletal dysplasia research in India.

Authors:  A Uttarilli; H Shah; A Shukla; K M Girisha
Journal:  J Postgrad Med       Date:  2018 Apr-Jun       Impact factor: 1.476

3.  Frequency of skeletal dysplasia in children with short stature presenting to endocrine clinic: An observational study.

Authors:  Saira Abbas; Muhammad Nadeem Ahsan; Muhammad Sohaib Asghar
Journal:  J Family Med Prim Care       Date:  2022-06-30

4.  Prenatal diagnosis of achondrogenesis type I: a case report.

Authors:  M Zeki Taner; Mertihan Kurdoglu; Cagatay Taskiran; M Anil Onan; Guven Gunaydin; Ozdemir Himmetoglu
Journal:  Cases J       Date:  2008-12-18
  4 in total

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