Literature DB >> 2650935

3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).

A Verloes1, M F Dresse, M Jovanovic, P Dodinval, F Geubelle.   

Abstract

We report a child with an unusual pattern of malformations: severe delay in bone maturation, wide fontanelles and facial dysmorphism (evoking cleidocranial dysplasia), relative macroencephaly with cerebellar vermis hypoplasia, hypertelorism, skeletal abnormalities (1st ribs aplasia, multifocal sternal ossification centers, thin bones), septal defect, muscular waste, hypotonia and developmental delay. Most of these features have been reported previously by Ritscher, Schinzel et al. in two sibs, who suffered more severe cerebellar malformations (Dandy-Walker cyst or vermis aplasia). We propose 3C syndrome as an easy acronym for this Cranio-Cerebello-Cardiac dysplasia.

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Year:  1989        PMID: 2650935     DOI: 10.1111/j.1399-0004.1989.tb02929.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.  A novel multiple congenital anomaly-mental retardation syndrome with Pierre Robin sequence and cerebellar hypoplasia in two sisters.

Authors:  David A Stevenson; John C Carey
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

3.  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 in total

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