Another family with tricho‐rhino‐phalangeal syndrome type III (Sugio‐Kajii syndrome)
- 1 February 1994
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 49 (3) , 278-280
- https://doi.org/10.1002/ajmg.1320490307
Abstract
Tricho‐rhino‐phalangeal syndrome Type III (TRPS III) is a newly defined genetic entity. Only 9 patients in a family and one sporadic patient have been reported. We add another family in which 4 individuals in 3 generations are affected with this autosomal dominant trait. Although they manifested short stature, sparse hair, “pear‐shaped” nose, and coneshaped epiphyses, sharing these findings with TRPS Type I, the presence of a severe form of generalized shortness of all phalanges and metacarpals, and the absences of mental deficiency and exostoses in this family distinguish the disorder from the TRPS Types I and II. Their manifestations are quite similar to those of the patients reported as TRPS III (Sugio‐Kajii syndrome).Keywords
This publication has 6 references indexed in Scilit:
- Tricho‐rhino‐phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3–24.13American Journal of Medical Genetics, 1989
- A final word on the tricho‐rhino‐phalangeal syndromesClinical Genetics, 1987
- The Sugio‐Kajii syndrome, proposed tricho‐rhino‐phalangeal syndrome type IIIAmerican Journal of Medical Genetics, 1986
- Ruvalcaba syndromeAmerican Journal of Medical Genetics, 1985
- Ruvalcaba syndrome: Autosomal dominant inheritanceAmerican Journal of Medical Genetics, 1984
- Tricho-rhino-phalangeal syndrome associated with perthes-disease-like bone change and spondylolisthesisJournal of Human Genetics, 1978