Literature DB >> 8831131

Melnick-Needles syndrome in a mother and her son.

P Neou1, S Kyrkanides, E Gioureli, C S Bartsocas.   

Abstract

The Melnick-Needles syndrome is a rare connective tissue disorder characterised by specific facial features (small facial bones, exophthalmos, hypertelorism, full checks 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.

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Year:  1996        PMID: 8831131

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  2 in total

1.  A Japanese case of oto-palato-digital syndrome type II: an apparent lack of phenotype-genotype correlation.

Authors:  T Kondoh; N Okamoto; N Norimatsu; M Uetani; G Nishimura; H Moriuchi
Journal:  J Hum Genet       Date:  2007-01-31       Impact factor: 3.172

2.  Melnick-Needles syndrome associated with growth hormone deficiency: a case report.

Authors:  Leyla Akın; Erdal Adal; Mustafa Ali Akın; Selim Kurtoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-08-07
  2 in total

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