Cutis laxa in Kabuki make-up syndrome
- 30 November 2005
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 53 (5) , S247-S251
- https://doi.org/10.1016/j.jaad.2005.02.007
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- On the reported 8p22‐p23.1 duplication in Kabuki make‐up syndrome (KMS) and its absence in patients with typical KMSAmerican Journal of Medical Genetics Part A, 2004
- Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndromeAmerican Journal of Medical Genetics Part A, 2004
- Unmasking Kabuki syndrome: chromosome 8p22–8p23.1 duplication revealed by comparative genomic hybridization and BAC‐FISHClinical Genetics, 2003
- Kabuki make‐up syndrome: A reviewAmerican Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2002
- Kabuki syndrome: a review study of three hundred patientsClinical Dysmorphology, 2002
- Congenital heart defects in Kabuki syndromeAmerican Journal of Medical Genetics, 2001
- Kabuki make‐up (Niikawa‐Kuroki) syndrome in the Byelorussian register of congenital malformations: Ten new observationsAmerican Journal of Medical Genetics, 1995
- Kabuki make‐up (Niikawa‐Kuroki) syndrome: A study of 62 patientsAmerican Journal of Medical Genetics, 1988
- A new malformation syndrome of long palpebralfissures, large ears, depressed nasal tip, and skeletal anomalies associated with postnatal dwarfism and mental retardationThe Journal of Pediatrics, 1981
- Kabuki make-up syndrome: A syndrome of mentalretardation, unusual facies, large and protruding ears, and postnatal growth deficiencyThe Journal of Pediatrics, 1981