Asymptomatic symmetrical hyperphalangism of the fingers accompanied by foot anomalies is very rare. We present a 21-year-old man with anomalies in both hands and feet. [ncbi.nlm.nih.gov]

Download PDF Download PDF (TR) Previous article in issue Next article in issue Vol 44, No 1 (2010) Pages :79-81 Hyperphalangism accompanied by brachydactyly of the feet: a case report S S Suresh, Raju Abraham Abstract Asymptomatic symmetrical hyperphalangism [aott.org.tr]

The SLAC wrist: scapholunate advanced collapse pattern of degenerative Arthritis. J Hand Surg [Am] 1984: 9-A:358-65. ‎ Pagina 308 - Arnett FC, Edworthy SM, Bloch DA. McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS. [books.google.ro]

The SLAC wrist: scapholunate advanced collapse pattern of degenerative Arthritis. J Hand Surg [Am] 1984: 9-A:358-65. ‎ Seite 308 - Arnett FC, Edworthy SM, Bloch DA. McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS. [books.google.de]

She had a high arching palate with no defect. Cervical spine and cardiac examinations revealed no abnormality. The upper extremities were of equal length. [docslide.com.br]

Type your tag names separated by a space and hit enter Links Publisher Full Text Authors Source MeSH Abnormalities, Multiple Child, Preschool Female Follow-Up Studies Foot Deformities, Congenital Hand Deformities, Congenital Humans Infant Infant, Newborn [unboundmedicine.com]

Upton’s practice is one of the world’s largest specializing in congenital hand deformities, vascular anomalies, and pediatric and adult microsurgery. [books.google.ro]

Inheritance MacKinder [ 29 ] described this hand deformity in six generations of a family. All studied cases in the literature demonstrated an autosomal dominant pattern of inheritance with variable severity. [ojrd.biomedcentral.com]

Wilder RL, Hunder GG: The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. ‎ [books.google.ro]

SUBSTANCE: hip joint unload technique aims at prevention and treatment of hip arthropathy ensured by complex exercise therapy and at prevention of hip arthrosis and arthritis provided by complex exercise therapy of lower limbs while lying on the back [russianpatents.com]

[…] hyperphalangism — hy·per·pha·lan·gism … English syllables List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity [useful_english.enacademic.com]

[…] phalanges in fingers or toes … Useful english dictionary List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity [medicine.academic.ru]

Because he had a similarly affected brother and his parents were cousins we suggest autosomal recessive inheritance, X-linked recessive inheritance cannot be excluded. [doi.org]

On the basis of ours and the three previous cases, the existence of a new palato-digital syndrome is suggested. یک پسر بچه نه روزه که سندرم پیر رابین نیز تا به حال ناهنجاری دست ناشی از غیر معمول متشکل از clinodactyly دوجانبه انگشت بود. [scipers.com]

On the basis of ours and the three previous cases, the existence of a new palato-digital syndrome is suggested. [link.springer.com]

Jones [ 16 ] suggested the designation "delta phalanx" for the triangular middle phalanx. [ojrd.biomedcentral.com]

The same hand malformation has been previously described in three patients who had either the Pierre Robin syndrome or isolated cleft palate. [scipers.com]

Farnsworth P, et a1: Glossoptotic hypoxia and micro-gnathia: The Pierre Robin Syndrome Reviewed. Clin Ped 10:600, 1971 8. Holthusen W, et al: The Pierre Robin syndrome: Unusual associated developmental defects. Ann Radiol 15:253, 1972 9. [docslide.com.br]

,, ,, ,, Source MeSH Hand Deformities, Congenital Humans Mutation Phosphoric Monoester Hydrolases Pierre Robin Syndrome Pub Type(s) Journal Article Language eng PubMed ID 22887726 TY - JOUR T1 - IMPAD1 mutations in two Catel-Manzke like patients. [unboundmedicine.com]

The index and middle fingers show hyperphalangism, which is confused occasionally with nonunion of a fracture. [ncbi.nlm.nih.gov]