Abstract
A male infant is described with severe micrognathia and bilateral duplication of the proximal phalanges of the index fingers, an association which is characteristic of the Catel-Manzke syndrome. In addition, he had dislocatable knees, which have not been described in this disorder before.
Full text
PDF
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Farnsworth P. B., Pacik P. T. Glossoptotic hypoxia and micrognathia--the Pierre Robin syndrome reviewed. Early recognition and prompt surgical treatment is important for survival. Clin Pediatr (Phila) 1971 Oct;10(10):600–606. doi: 10.1177/000992287101001029. [DOI] [PubMed] [Google Scholar]
- Gewitz M., Dinwiddie R., Yuille T., Hill F., Carter C. O. Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence. J Med Genet. 1978 Apr;15(2):162–164. doi: 10.1136/jmg.15.2.162. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holthusen W. [The Pierre Robin syndrome: unusual associated developmental defects]. Ann Radiol (Paris) 1972 Mar-Apr;15(3):253–262. [PubMed] [Google Scholar]
- Lipson A., Beuhler B., Bartley J., Walsh D., Yu J., O'Halloran M., Webster W. Maternal hyperphenylalaninemia fetal effects. J Pediatr. 1984 Feb;104(2):216–220. doi: 10.1016/s0022-3476(84)80995-6. [DOI] [PubMed] [Google Scholar]
- Manzke H. Symmetrische Hyperphalangie des zweiten Fingers durch ein akzessorisches Metacarpale. Fortschr Geb Rontgenstr Nuklearmed. 1966 Sep;105(3):425–427. [PubMed] [Google Scholar]
- Silengo M. C., Franceschini P., Cerutti A., Fabris C. Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome. Pediatr Radiol. 1977 Oct 28;6(3):178–180. doi: 10.1007/BF00972113. [DOI] [PubMed] [Google Scholar]
- Stevenson R. E., Huntley C. C. Congenital malformations in offspring of phenylketonuric mothers. Pediatrics. 1967 Jul;40(1):33–45. [PubMed] [Google Scholar]
- Stevenson R. E., Taylor H. A., Jr, Burton O. M., Hearn H. B., 3rd A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton. J Med Genet. 1980 Jun;17(3):238–242. doi: 10.1136/jmg.17.3.238. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sundaram V., Taysi K., Hartmann A. F., Jr, Shackelford G. D., Keating J. P. Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel-Manzke syndrome. A case report and review of the literature. Clin Genet. 1982 Jun;21(6):407–410. doi: 10.1111/j.1399-0004.1982.tb01395.x. [DOI] [PubMed] [Google Scholar]