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Spectrum of severe skeletal dysplasias in North India

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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.

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References

  1. Andersen PE. Prevalence of lethal osteochondrodysplasias in Denmark. Am J Med Genet 1989; 32: 484–489.

    Article  PubMed  Google Scholar 

  2. Connor JM, Connor RAC, Sweet AAM, Patrick WJA, McNay MB, Redford DHA. Lethal neonatal chondrodysplasias in the west of Scotland 1970–1983 with a description of a thanatophoric dysplasia-like autosomal recessive disorder, Glasgow variant. Am J Med Genet 1985; 22: 243–253.

    Article  PubMed  CAS  Google Scholar 

  3. Parilla BV, Leeth EA, Kambich MP, Chilis P, MacGregor SN. Antenatal Detection of Skeletal Dysplasias. J Ultrasound Med 2003; 22: 255–258.

    PubMed  Google Scholar 

  4. Rahemtullah A, McGillivray B, Wilson RD. 1997. Suspected skeletal dysplasias: Femur length to abdominal circumference ratio can be used in ultrasonographic prediction of fetal outcome. Am J Obstet Gynecol 177: 864–869.

    Article  PubMed  CAS  Google Scholar 

  5. Tretter AE, Saunders RC, Meyers CM, Dungan JS, Grumbach K, Sun CC et al. Antenatal Diagnosis of Lethal Skeletal Dysplasias. Am J Med Genet 1998; 75: 518–522.

    Article  PubMed  CAS  Google Scholar 

  6. Rasmussen SA, Bieber FR, Benacerraf BR, Lachman RS, Rimoin DL, Holmes LB. Epidemiology of osteochondrodysplasias: Changing trends due to advances in prenatal diagnosis. Am J Med Genet 1996; 61: 49–58.

    Article  PubMed  CAS  Google Scholar 

  7. Cassart M, Massez A, Cos T, Tecco L, Thomas D, Van Regemorter N et al. Contribution of three-dimensional computed tomography in the assessment of fetal skeletal dysplasia. Ultrasound Obstet Gynecol 2007; 29: 537–543.

    Article  PubMed  CAS  Google Scholar 

  8. Sharony R, Browne C, Lachman RS, Rimoin DL. Prenatal diagnosis of the skeletal dysplasias. Am J Obstet Gynecol 1993; 169: 668–675.

    PubMed  CAS  Google Scholar 

  9. Verma, IC, Bhargava S, Agarwal S. A lethal chondrodystrophy with severe thoracic dystrophy, rhizoacromelic type of micromelia, polydactyly and genital anomalies. In Disorders of Connective Tissue, edited by D. Bergsma Birth Defects Org Art Ser, vol XI no. 6, New York; 1975; 167–174. National Foundation, March of Dimes.

    Google Scholar 

  10. Sridhar S, Kishore R, Thomas N, Jana AK. Short rib polydactyly syndrome-Type I. Indian J Pediatr 2004; 71: 359–361.

    Article  PubMed  CAS  Google Scholar 

  11. Verma A. Short rib polydactyly syndrome type I (Saldino-Noonan syndrome). Indian Pediatr 2005; 42: 389.

    PubMed  Google Scholar 

  12. Malhotra N, Sood M. Recurrence of short rib polydactyly syndrome — a rare skeletal dysplasia. Eur J Obstet Gynecol Reprod Biol 2000; 89: 193–195.

    Article  PubMed  CAS  Google Scholar 

  13. Lavanya R, Pratap K. Short rib polydactyly syndrome—a rare skeletal dysplasia. Int J Gynaecol Obstet 1995; 50: 291–292.

    Article  PubMed  CAS  Google Scholar 

  14. Sharma AK, Phadke SR, Agarwal SS. Short rib (polydactyly) syndrome type IV: Beemer-Langer syndrome. Am J Med Genet 1993 15;46: 345–346.

    Article  Google Scholar 

  15. Beales PL, Bland E, Tobin JL, Bacchelli C, Tuysuz B, Hill J, Rix S, et al. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy. Nat Genet 2007; 39(6): 727–729.

    Article  PubMed  CAS  Google Scholar 

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Correspondence to I. C. Verma.

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Puri, R.D., Thakur, S. & Verma, I.C. Spectrum of severe skeletal dysplasias in North India. Indian J Pediatr 74, 995–1002 (2007). https://doi.org/10.1007/s12098-007-0183-y

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  • DOI: https://doi.org/10.1007/s12098-007-0183-y

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