Literature DB >> 1606716

An additional patient with the 3C syndrome.

F Gurrieri1, G Neri.   

Abstract

We report on an 8-month-old child with a dolichocephalic head due to prominent forehead and occiput. Dandy-Walker malformation, cleft palate, congenital heart defect and other minor anomalies. He represents a new case of the 3C syndrome, the fifth described in the medical literature.

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Year:  1992        PMID： 1606716     DOI： 10.1111/j.1399-0004.1992.tb03678.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  3 in total

1.  Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

Authors:  M G Butler; P Mowrey
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

2.  Another case of Ritscher-Schinzel-syndrome: craniocerebello-cardiac dysplasia (3C-syndrome) with associated bilateral colobomata.

Authors:  H Wörle; M A Lewin; M Holder; C K Bastanier; B Köhler
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

3.  A rare case of 3C disease: Ritscher-Schinzel syndrome presenting with recurrent talipes equinovarus.

Authors:  Mehmet Nuri Konya; Muhsin Elmas; Sadık Emre Erginoğlu; Murat Yeşil
Journal:  Int J Surg Case Rep       Date:  2014-11-06
  3 in total

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