Literature DB >> 6893487

Syndrome of hydrocephalus, costovertebral dysplasia and Sprengel anomaly with autosomal dominant inheritance.

P E Waaler, D Aarskog.   

Abstract

A malformation syndrome affecting a mother and her three daughters is reported. The patients showed various combinations of the following malformations and anomalies: spontaneously arrested communicating hydrocephalus, costovertebral dysplasia, Sprengel anomaly (undescended scapula), hypertelorism, broad and low nasal bridge, anteverted nostrils, low-set ears, high-arched palate, prominent mandibula, enamel hypoplasia and increased interspace between the 1st and 2nd toes. The occurrence of similar abnormalities in the mother and her three daughters and the variable expression of the manifestations indicate that the syndrome was inherited as an autosomal dominant trait.

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Year:  1980        PMID: 6893487     DOI: 10.1055/s-2008-1071398

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  2 in total

1.  Neuropathology of congenital hydrocephalus in the SUMS/NP mouse.

Authors:  J E Bruni; M R del Bigio; E R Cardoso; T V Persaud
Journal:  Acta Neurochir (Wien)       Date:  1988       Impact factor: 2.216

2.  Subperiosteal resection of mid-clavicle in Sprengel's deformity correction.

Authors:  Freih Odeh Abuhassan
Journal:  Strategies Trauma Limb Reconstr       Date:  2011-07-20
  2 in total

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