Literature DB >> 3692880

The 3-M syndrome. A heritable low birthweight dwarfism.

H Van Goethem1, P Malvaux.   

Abstract

Two male siblings and one girl with the 3-M syndrome are reported. The main clinical features include low birthweight, proportionate dwarfism, hatched-shaped cranio-facial configuration, abnormalities of mouth and teeth, short broad neck with prominent trapezius, pectus deformity, transverse grooves of anterior chest, and winged scapulae.

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Year:  1987        PMID: 3692880

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  2 in total

1.  Dwarfism with gloomy face: a new syndrome with features of 3-M syndrome.

Authors:  M Le Merrer; R Brauner; P Maroteaux
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

2.  3-M syndrome associated with growth hormone deficiency: 18 year follow-up of a patient.

Authors:  Cristina Meazza; Ekkehard Lausch; Sara Pagani; Elena Bozzola; Valeria Calcaterra; Andrea Superti-Furga; Margherita Silengo; Mauro Bozzola
Journal:  Ital J Pediatr       Date:  2013-03-21       Impact factor: 2.638

  2 in total

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