Literature DB >> 1513756

A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)

M I Tejada1, A Uribarren, P Briones, M A Vilaseca.   

Abstract

A case of mosaic tetrasomy 12p was detected in amniotic fluid cell cultures from a 28-year-old woman referred to us at 26 weeks' gestation because of hydramnios. The fetus was shown on ultrasonography to have an omphalocele and a short femur length. Labour was induced at 32 weeks. An infant with multiple congenital anomalies was delivered and died after 10 min. The diagnosis of i(12p) or Pallister-Killian syndrome was confirmed cytogenetically in fibroblast and lymphocyte cultures. Increased LDH-B activity was demonstrated in fibroblasts.

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Year:  1992        PMID: 1513756     DOI: 10.1002/pd.1970120608

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  1 in total

1.  Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.

Authors:  D Horn; F Majewski; B Hildebrandt; H Körner
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

  1 in total

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