Limited joint mobility

Diabetic cheiroarthropathy, also known as Diabetic stiff hand syndrome or limited joint mobility syndrome, is a cutaneous condition characterized by waxy, thickened skin and limited joint mobility of the hands and fingers, leading to flexion contractures, a condition associated with diabetes mellitus and it is observed in roughly 30% of diabetic patients with longstanding disease. It can be a predictor for other diabetes-related complications and was one of the earliest known complications of diabetes, first documented in 1974.In the fingers, diabetic cheiroarthropathy can cause such extreme limited mobility that the patient is unable to fully extend the fingers in order to flatten the hand. [Source: Wikipedia ]

Joint contracture
May Be Caused by
Aase-Smith syndrome
Addison disease
Allan-Herndon-Dudley syndrome
Ankylosed thumbs and mental retardation
Antley-Bixler syndrome
Apert syndrome
Aplasia cutis congenita
Bee-keeper arthropathy
Brachmann-de Lange syndrome
Bruck syndrome
Carpotarsal osteochondromatosis
Cerebro-oculofacioskeletal syndrome
Chondrodysplasia punctata Conradi-Hünermann type
Chondrodysplasia punctata rhizomelic type
Christian syndrome
Cockayne syndrome
Contractural arachnodactyly
Debuquois dysplasia
Dermochondrocorneal dystrophy of François
Diabetes mellitus
Diastrophic dysplasia
Digitotalar dysmorphism
Distal arthrogryposis type 2A
Duchenne muscular dystrophy
Dyggve-Melchior-Clausen dysplasia
Dysplasia epiphysealis hemimelica
Dyssegmental dysplasia
Emery-Nelson syndrome
Epidermolysis bullosa dystrophica
Fabry disease
Familial arachnodactyly-distal arthrogryposis
Farber disease
Femoral hypoplasia-unusual facies syndrome
Fetal akinesia sequence
Fetal alcohol syndrome
Fibrodysplasia ossificans progressiva
Frontometaphyseal dysplasia
Geleophysic dysplasia
GEMSS syndrome
German syndrome
GM1 gangliosidosis
Goldberg-Shprintzen syndrome
Golden-Lakim syndrome
Gordon syndrome
Hereditary multiple exostoses
Infantile multisystem inflammatory disease
Klein-Waardenburg syndrome
Kniest dysplasia
Kuskokwim syndrome
Kyphomelic dysplasia
Léri syndrome
Lin-Gettig syndrome
Macrodystrophia lipomatosa
Mandibuloacral dysplasia
Marden-Walker syndrome
Meier-Gorlin syndrome
Mesomelic dysplasia Nievergelt type
Metaphyseal chondrodysplasia Jansen type
Metatropic dysplasia
Mietens-Weber syndrome
Mixed connective tissue disease
Moore-Federman syndrome
Multiple epiphyseal dysplasia
Multiple synostosis syndrome
Myhre syndrome
Nail-patella syndrome
Nevo syndrome
Osebold-Remondini dysplasia
Osteogenesis imperfecta
Parastremmatic dysplasia
Pelvic dysplasia - arthrogrypotic lower limbs
Progressive pseudorheumatoid chondrodysplasia
Pseudodiastrophic dysplasia
Pterygium syndrome
Renal-coloboma syndrome
Rigid spine syndrome
Rutledge syndrome
Schwartz-Jampel syndrome
Seckel syndrome
Short stature, contractures, upper body pterygia, brachydactyly
Sjögren-Larsson syndrome
Spondyloepimetaphyseal dysplasia
Spondyloepimetaphyseal dysplasia dominant metatropic type
Spondyloepimetaphyseal dysplasia Irapa type
Spondyloepiphyseal dysplasia tarda
Stewart-Bergstrom syndrome
Stickler syndrome
Stiff skin syndrome
Stiff-man syndrome
Symphalangism-surdity syndrome
TAC syndrome
Tattoo dysplasia
Trismus-pseudocamptodactyly syndrome
Trisomy 13
Trisomy 18
Trisomy 8
Tumoral calcinosis
Van den Ende-Gupta syndrome
Weill-Marchesani syndrome
Winchester syndrome
X-linked mental retardation with clasped thumbs
XXXXY syndrome
Zellweger syndrome