CASE OF SYNDROME OF CORNELIA DE LANGE (CLINICAL OBSERVATIONS).

Authors

  • O. V. Omelchenko
  • A. F. Shypko
  • M. I. Strelkova

DOI:

https://doi.org/10.11603/24116-4944.2015.1.4674

Abstract

The article is devoted to rare syndrome of uncertain course of succession. Describes the etiology, phenotypic characteristics, symptoms, based on which a pediatrician and geneticist may suspect the Amsterdam dwarfism. Principles of treatment summarize the general. Clinical observation of the child V. 6 years old with multiple organ failure was conducted.

References

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Гинтер Е. К. Медицинская генетика / Е. К. Гинтер . - М . : Медицина, 2003. - 448 с.

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Козлова С. И. Наследственные синдромы и медико-генетическое консультирование / С. И. Козлова, Н. С. Демикова. - М., 2007. - 254 с.

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Published

2015-07-17

How to Cite

Omelchenko, O. V., Shypko, A. F., & Strelkova, M. I. (2015). CASE OF SYNDROME OF CORNELIA DE LANGE (CLINICAL OBSERVATIONS). Actual Problems of Pediatrics, Obstetrics and Gynecology, (1). https://doi.org/10.11603/24116-4944.2015.1.4674

Issue

No. 1 (2015)

Section

PEDIATRICS

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