[Surgical treatment of syndactylia in recessive epidermolysis bullosa dystrophica]. 1988

A Lamesch, and J Reiffers

UI MeSH Term Description Entries
D008297 Male Males
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003286 Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. Contractures
D004820 Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. Acantholysis Bullosa
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D013576 Syndactyly A congenital anomaly of the hand or foot, marked by the webbing between adjacent fingers or toes. Syndactylies are classified as complete or incomplete by the degree of joining. Syndactylies can also be simple or complex. Simple syndactyly indicates joining of only skin or soft tissue; complex syndactyly marks joining of bony elements. Polysyndactyly,Syndactylia,Syndactylias,Syndactylies

Related Publications

A Lamesch, and J Reiffers
October 1985, Laryngologie, Rhinologie, Otologie,
A Lamesch, and J Reiffers
January 1978, The Tohoku journal of experimental medicine,
A Lamesch, and J Reiffers
August 1988, Rinsho hoshasen. Clinical radiography,
A Lamesch, and J Reiffers
November 1982, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons,
A Lamesch, and J Reiffers
January 1946, Dermatologica,
A Lamesch, and J Reiffers
June 1971, Birth defects original article series,
A Lamesch, and J Reiffers
July 1951, A.M.A. archives of dermatology and syphilology,
A Lamesch, and J Reiffers
January 1937, Proceedings of the Royal Society of Medicine,
Copied contents to your clipboard!