Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel‐Manzke syndrome. A case report and review of the literature
1982; Wiley; Volume: 21; Issue: 6 Linguagem: Inglês
10.1111/j.1399-0004.1982.tb01395.x
ISSN1399-0004
AutoresVasantha Sundaram, Kutay Taysi, Alica Hartmann, Gary D. Shackelford, James Keating,
Tópico(s)Oral and Craniofacial Lesions
ResumoMandibular hypoplasia, glossoptosis, U‐shaped cleft palate (Pierre Robin anomaly), associated with bilateral index finger malformation and congenital heart disease are described in a male, newborn infant. Review of the features of seven previously published patients, in addition to the patient reported here, confirms the existence of a distinct dysmorphogenesis syndrome. Although all of these eight patients have been males, and most were sporadic, the etiology of this rare malformation syndrome is unknown.
Referência(s)