Our website is made possible by displaying online advertisements to our visitors.
Please consider supporting us by disabling your ad blocker.

Responsive image


Camptodactyly

Camptodactyly
Pronunciation
  • kamp-to-dak-tee-lee
SpecialtyMedical genetics
SymptomsPermanent flexion of the proximal interphalangeal joints, although symptoms may vary in person; some people have very tight flexed fingers and other people have flexed fingers that straighten when pressed on [1]
ComplicationsPeople with severe camptodactyly may have difficulty holding objects
Usual onsetThere are congenital forms, adolescent-onset forms and acquired forms [2]
DurationLife-long
TreatmentSplinting, surgery, etc.
Frequency1% of the world population [3] [4] [5]

Camptodactyly is a medical condition that causes one or more digits (fingers or toes) to be permanently bent. It involves fixed flexion deformity of the proximal interphalangeal joints.

Camptodactyly can be caused by a genetic disorder. In that case, it is an autosomal dominant trait that is known for its incomplete genetic expressivity. This means that when a person has the genes for it, the condition may appear in both hands, one, or neither. A linkage scan proposed that the chromosomal locus of camptodactyly was 3q11.2-q13.12.[6]

  1. ^ "Camptodactyly | Boston Children's Hospital". Archived from the original on 2021-11-16.
  2. ^ "Camptodactyly | Boston Children's Hospital". Archived from the original on 2021-11-16.
  3. ^ "Camptodactyly - Hand - Orthobullets". Archived from the original on 2021-08-04.
  4. ^ "Camptodactyly". 18 November 2016. Archived from the original on 2021-06-21.
  5. ^ Ravishanker, R; Bath, AS (July 2004). "Distraction - A Minimally Invasive Technique for Treating Camptodactyly and Clinodactyly". Medical Journal, Armed Forces India. 60 (3): 227–230. doi:10.1016/S0377-1237(04)80051-0. PMC 4923171. PMID 27407638.
  6. ^ Malik, Sajid; Schott, Jörg; Schiller, Julia; Junge, Anna; Baum, Erika; Koch, Manuela C. (February 2008). "Fifth finger camptodactyly maps to chromosome 3q11.2–q13.12 in a large German kindred". European Journal of Human Genetics. 16 (2): 265–9. doi:10.1038/sj.ejhg.5201957. PMID 18000522.

Previous Page Next Page