Literature DB >> 2801769

RAPADILINO syndrome with radial and patellar aplasia/hypoplasia as main manifestations.

H Kääriäinen1, S Ryöppy, R Norio.   

Abstract

A new malformation syndrome is described in a pair of sibs and 3 sporadic patients. The characteristic manifestations are radial aplasia or hypoplasia, absence of thumbs, absent or hypoplastic patellae, dislocations of joints, unusual face, cleft or highly arched palate, diarrhea in infancy, small stature, and normal intelligence. Recessive inheritance seems the most plausible cause. The acronym RAPADILINO syndrome is proposed.

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Mesh:

Year:  1989        PMID: 2801769     DOI: 10.1002/ajmg.1320330312

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


  17 in total

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Authors:  K L Greenhalgh; R T Howell; A Bottani; P J Ancliff; H G Brunner; C C Verschuuren-Bemelmans; E Vernon; K W Brown; R A Newbury-Ecob
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6.  Report of Two Novel Mutations in Indian Patients with Rothmund-Thomson Syndrome.

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7.  Vascularized metatarsophalangeal joint transfer for radial hypoplasia.

Authors:  Simo K Vilkki
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Review 8.  Rothmund-Thomson syndrome.

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Review 9.  Roles of Werner syndrome protein in protection of genome integrity.

Authors:  Marie L Rossi; Avik K Ghosh; Vilhelm A Bohr
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10.  RAPADILINO RECQL4 mutant protein lacks helicase and ATPase activity.

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Journal:  Biochim Biophys Acta       Date:  2012-07-31
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