Camptodactyly

Camptodactyly is a medical condition that causes one or more fingers to be permanently bent. It involves fixed flexion deformity of the proximal interphalangeal joints. [Source: Wikipedia ]

Synonyms
Flexion deformity of one or more digits
May Cause
Contracture of a digit
May Be Caused by
Aarskog syndrome
Acro-fronto-facio-nasal dysostosis
Aicardi syndrome
Ainhum
Antley-Bixler syndrome
Arthritis
Arthrogryposis
Arthropathy-camptodactyly syndrome
Blau syndrome
Camptobrachydactyly
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia
Camptodactyly - joint contractures - facial skeletal defects
Camptodactyly - tall stature - scoliosis - hearing loss
Camptodactyly - taurinuria
Camptodactyly-ankylosis-pulmonary hypoplasia syndrome
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Camptodactyly-eye syndrome
Camptodactyly-ichthyosis syndrome
Cerebro-oculo-facio-skeletal syndrome
Cerebrofacioauricular syndrome of Van Maldergem
CHARGE syndrome
Christian syndrome
Congenital contractural arachnodactyly
Contractural arachnodactyly
Craniofrontonasal dysplasia
Crisponi syndrome
Da Silva syndrome
Digital fibroma
Distal arthrogryposis
Distal arthrogryposis type 2A
Dupuytren contracture
Faciothoracoskeletal syndrome
Familial camptodactyly
Familial camptodactylyscoliosis
Familial fibrosing serositis
Fetal akinesia deformation sequence
Fetal akinesia sequence
Fetal alcohol syndrome
Fracture
Frank-ter Haar syndrome
Fryns syndrome
Goldberg-Shprintzen syndrome
Golden-Lakim syndrome
Goltz syndrome
Goodman syndrome
Gordon syndrome
Grebe chondrodysplasia
Greig cephalopolysyndactyly syndrome
Guadalajara camptodactyly type 1
Guadalajara camptodactyly type 2
Guadalajara camptodactyly type 3
Holt-Oram syndrome
Infection
Isolated absence of phalanx
Isolated hypoplasia of phalanx
Klein-Waardenburg syndrome
Kuskokwim syndrome
Kyphomelic dysplasia
Lacrimo-auriculo-dento-digital syndrome
LAPS syndrome
Lenz microphthalmia syndrome
Lin-Gettig syndrome
Marden-Walker syndrome
Marfan syndrome
MCA syndrome
Meckel syndrome
Mesomelic dwarfism - cleft palate - camptodactyly
Mesomelic dysplasia with spur-limbs
Monosomy 21 syndrome
Nail-patella syndrome
Neoplasm
Neu-Laxova syndrome
Noonan syndrome
Oculo-dento-osseous dysplasia
Ophthalmomandibulomelic dysplasia
Orofaciodigital syndrome type 1
Otopalatodigital syndrome type 2
Pashayan-Pruzansky syndrome
Pointer syndrome
Poland syndrome
Popliteal pterygium syndrome
Progeria
Pseudodiastrophic dysplasia
Rheumatoid arthritis
Roberts syndrome
Silver-Russell syndrome
Spondylocostal dysostosis
Stewart-Bergstrom syndrome
Stratton-Parker syndrome
Stüve-Wiedemann dysplasia
Teebi-Shaltout syndrome
Tel Hashomer camptodactyly syndrome
Thermal injury
Trauma
Triploidy
Trismus-pseudocamptodactyly syndrome
Trisomy 13
Trisomy 18
Trisomy 21
Trisomy 8
Volkmann contracture
W syndrome
Weaver syndrome
Williams syndrome
Zellweger syndrome
Flexion deformity of one or more digits
Aarskog syndrome
Acro-fronto-facio-nasal dysostosis
Aicardi syndrome
Ainhum
Antley-Bixler syndrome
Arthritis
Arthrogryposis
Arthropathy-camptodactyly syndrome
Blau syndrome
Camptobrachydactyly
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia
Camptodactyly - joint contractures - facial skeletal defects
Camptodactyly - tall stature - scoliosis - hearing loss
Camptodactyly - taurinuria
Camptodactyly-ankylosis-pulmonary hypoplasia syndrome
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Camptodactyly-eye syndrome
Camptodactyly-ichthyosis syndrome
Cerebro-oculo-facio-skeletal syndrome
Cerebrofacioauricular syndrome of Van Maldergem
CHARGE syndrome
Christian syndrome
Congenital contractural arachnodactyly
Contractural arachnodactyly
Craniofrontonasal dysplasia
Crisponi syndrome
Da Silva syndrome
Digital fibroma
Distal arthrogryposis
Distal arthrogryposis type 2A
Dupuytren contracture
Faciothoracoskeletal syndrome
Familial camptodactyly
Familial camptodactylyscoliosis
Familial fibrosing serositis
Fetal akinesia deformation sequence
Fetal akinesia sequence
Fetal alcohol syndrome
Fracture
Frank-ter Haar syndrome
Fryns syndrome
Goldberg-Shprintzen syndrome
Golden-Lakim syndrome
Goltz syndrome
Goodman syndrome
Gordon syndrome
Grebe chondrodysplasia
Greig cephalopolysyndactyly syndrome
Guadalajara camptodactyly type 1
Guadalajara camptodactyly type 2
Guadalajara camptodactyly type 3
Holt-Oram syndrome
Infection
Isolated absence of phalanx
Isolated hypoplasia of phalanx
Klein-Waardenburg syndrome
Kuskokwim syndrome
Kyphomelic dysplasia
Lacrimo-auriculo-dento-digital syndrome
LAPS syndrome
Lenz microphthalmia syndrome
Lin-Gettig syndrome
Marden-Walker syndrome
Marfan syndrome
MCA syndrome
Meckel syndrome
Mesomelic dwarfism - cleft palate - camptodactyly
Mesomelic dysplasia with spur-limbs
Monosomy 21 syndrome
Nail-patella syndrome
Neoplasm
Neu-Laxova syndrome
Noonan syndrome
Oculo-dento-osseous dysplasia
Ophthalmomandibulomelic dysplasia
Orofaciodigital syndrome type 1
Otopalatodigital syndrome type 2
Pashayan-Pruzansky syndrome
Pointer syndrome
Poland syndrome
Popliteal pterygium syndrome
Progeria
Pseudodiastrophic dysplasia
Rheumatoid arthritis
Roberts syndrome
Silver-Russell syndrome
Spondylocostal dysostosis
Stewart-Bergstrom syndrome
Stratton-Parker syndrome
Stüve-Wiedemann dysplasia
Teebi-Shaltout syndrome
Tel Hashomer camptodactyly syndrome
Thermal injury
Trauma
Triploidy
Trismus-pseudocamptodactyly syndrome
Trisomy 13
Trisomy 18
Trisomy 21
Trisomy 8
Volkmann contracture
W syndrome
Weaver syndrome
Williams syndrome
Zellweger syndrome