Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome

Hakan N., Eminoglu F. T., Aydin M., Zenciroglu A., Karadag N. N., Dursun A., ...More

Congenital Anomalies, vol.52, no.4, pp.216-218, 2012 (SCI-Expanded, Scopus) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 52 Issue: 4
  • Publication Date: 2012
  • Doi Number: 10.1111/j.1741-4520.2012.00360.x
  • Journal Name: Congenital Anomalies
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.216-218
  • Keywords: camptodactyly, Crisponi syndrome, CRLF1 gene, hypertonia, mutation, SONIC HEDGEHOG, VACTERL-ASSOCIATION, ESOPHAGEAL ATRESIA, VATER ASSOCIATION, DEFECTS, GLI2, WNT, MORPHOGENESIS, DEFINITION, FISTULA
  • Lokman Hekim University Affiliated: No

Abstract

Crisponi syndrome is an infrequently described disorder with autosomal recessive trait. It is characterized by extensive muscular contractions in the face after even minimal stimuli or crying, hypertonia, opisthotonus, camptodactyly, and typical facial features. Muscle contractions attenuate during rest or when the infant calms down. As a recently described new disease, Crisponi syndrome may be confused with epileptic manifestations. Most of the patients die in the first months of life due to hyperthermia and feeding problems. Recently, it has been demonstrated that mutations of the CRLF1 gene 'cytokine receptor-like factor 1' are associated with Crisponi syndrome. Here, we present a newborn diagnosed with Crisponi syndrome and report a novel homozygous CFRL1 gene mutation. © 2012 The Authors. Congenital Anomalies © 2012 Japanese Teratology Society.