Literature DB >> 8140064

DNA confirmation of congenital myotonic dystrophy in non-immune hydrops fetalis.

R F Stratton1, R M Patterson.   

Abstract

We report on the prenatal diagnosis of congenital myotonic dystrophy in a case of non-immune hydrops fetalis. DNA analysis of amniocytes revealed expansion of the trinucleotide (CTG) repeat within the myotonin PK gene, associated with myotonic dystrophy. The fetus was found to have approximately 1730 copies, while the normal population has between 5 and 27 copies, and minimally affected individuals have at least 50 copies.

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Year:  1993        PMID: 8140064     DOI: 10.1002/pd.1970131104

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


  3 in total

1.  Diagnosis of non-immune hydrops in the newborn.

Authors:  P D Turnpenny
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1994-07       Impact factor: 5.747

Review 2.  A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Authors:  Anne H Mardy; Shilpa P Chetty; Mary E Norton; Teresa N Sparks
Journal:  Prenat Diagn       Date:  2019-06-26       Impact factor: 3.050

3.  A case report on 30-week premature twin babies with congenital myotonic dystrophy conceived by in vitro fertilization.

Authors:  Su Bin Son; Jung Mi Chun; Kyung Ah Kim; Sun Young Ko; Yeon Kyung Lee; Son Moon Shin
Journal:  J Korean Med Sci       Date:  2012-10-02       Impact factor: 2.153

  3 in total

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