Literature DB >> 2986457

A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.

A Richieri-Costa, G M Colletto, T R Gollop, D Masiero.   

Abstract

We describe two sibs born to a consanguineous couple. Among other clinical findings both have mental retardation, short stature, facial and skeletal abnormalities characterized by hypertelorism, broad notched nasal tip, cleft lip/palate, campto-brachy-poly-syndactyly, fibular hypoplasia, and marked anomalies of foot structures. Facial signs of the reported patients resemble those present in the fronto-nasal "dysplasia" syndrome; however, the whole clinical picture in the present patients suggests a true MCA/MR syndrome, most likely inherited as an autosomal recessive trait. Clinical and genetic aspects of the present family are discussed.

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Year:  1985        PMID: 2986457     DOI: 10.1002/ajmg.1320200409

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Two brothers with characteristic facial appearance, severe psychomotor retardation, hypospadias, contractures, and other symptoms: a new recessive syndrome?

Authors:  G Wolff; E Zimmermann; B Zimmerhackl; C Harnasch; C Jung; E Back
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

2.  Craniofrontonasal dysplasia.

Authors:  L Kapusta; H G Brunner; B C Hamel
Journal:  Eur J Pediatr       Date:  1992-11       Impact factor: 3.183

3.  Frontofacionasal Dysplasia in a Newborn with a De Novo Duplication of 7p15.2-p15.1.

Authors:  Tamer Mansour; Sainan Wei; Michael Netzloff; Tarek Mohamed; Brian Schutte; Said A Omar
Journal:  AJP Rep       Date:  2015-05-15
  3 in total

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