Neonatal paroxysmal trismus and camptodactyly: The Crisponi syndrome
- 6 January 2005
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 133A (1) , 90-92
- https://doi.org/10.1002/ajmg.a.30536
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 SyndromeAmerican Journal of Human Genetics, 2004
- Crisponi syndrome: Report of a further patientAmerican Journal of Medical Genetics Part A, 2003
- Stüve-Wiedemann syndrome in children surviving infancy: clinical and radiological featuresClinical Dysmorphology, 2003
- Autosomal recessive disorder with muscle contractions resembling neonatal tetanus, characteristic face, camptodactyly, hyperthermia, and sudden death: A new syndrome?American Journal of Medical Genetics, 1996