Melnick-needles syndrome in a mother and her son

P. Neou, S. Kyrkanides, E. Gioureli, C. S. Bartsocas

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The Melnick-Needles syndrome is a rare connective tissue disorder characterised by specific facial features (small facial bones, exophthalmos, hypertelorism, full cheeks and small mandible), skeletal defects and short stature. The syndrome is considered to be lethal in males. Nevertheless, five surviving males are considered to represent new mutations. We are presenting an affected surviving male with the Melnick-Needles syndrome born to an affected mother.

Original languageEnglish
Pages (from-to)123-129
Number of pages7
JournalGenetic Counseling
Volume7
Issue number2
StatePublished - 1996

Keywords

  • Melnick-Needles syndrome

ASJC Scopus subject areas

  • Genetics(clinical)

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