Sclerodactyly

Sclerodactyly is a localized thickening and tightness of the skin of the fingers or toes that yields a characteristic claw-like appearance and spindle shape of the affected digits, and renders them immobile or of limited mobility.[3] Sclerodactyly is often preceded by months or even years by Raynaud's phenomenon when it is part of systemic scleroderma.It is generally associated with systemic scleroderma and mixed connective tissue disease, and auto-immune disorders.Localized treatment won't halt systemic disease, but can restore function and cosmetic aspects of the affected digits.In other cases, early treatment while the disease is in the inflammatory stage is much more likely to be successful than on established lesions[citation needed].
SpecialtyDermatologythickening and tightnessfingersdigitsmorpheaconnective tissuemuscleRaynaud's phenomenonsystemic sclerodermamixed connective tissue diseaseauto-immune disorderslimited cutaneous form of systemic sclerosiscalcinosisesophageal dysmotilitytelangiectasiaHuriez Syndromediabetes mellitusHand eczemaAtopic dermatitisDiseasesDBEpidermal thickeningkeratodermaKeratoderma climactericumParaneoplastic keratodermaAcrokeratosis paraneoplastica of BazexAquagenic keratodermaDrug-induced keratodermapsoriasisKeratoderma blennorrhagicumkeratosisSeborrheic keratosisClonal seborrheic keratosisCommon seborrheic keratosisIrritated seborrheic keratosisSeborrheic keratosis with squamous atypiaReticulated seborrheic keratosisDermatosis papulosa nigraKeratosis punctata of the palmar creaseshyperkeratosisAcanthosis nigricansConfluent and reticulated papillomatosisCallusIchthyosis acquisitaArsenical keratosisChronic scar keratosisHyperkeratosis lenticularis perstansHydrocarbon keratosisHyperkeratosis of the nipple and areolaInverted follicular keratosisLichenoid keratosisMultiple minute digitate hyperkeratosisPUVA keratosisReactional keratosisStucco keratosisThermal keratosisViral keratosisWarty dyskeratomaWaxy keratosis of childhoodKeloidHypertrophic scarCutis verticis gyrataNecrobiosisgranulomaGranuloma annularePerforatingGeneralizedSubcutaneousGranuloma annulare in HIV diseaseLocalized granuloma annularePatch-type granuloma annulareNecrobiosis lipoidicaAnnular elastolytic giant-cell granulomaGranuloma multiformeNecrobiotic xanthogranulomaPalisaded neutrophilic and granulomatous dermatitisRheumatoid nodulosisInterstitial granulomatous dermatitisInterstitial granulomatous drug reactionForeign body granulomaBeryllium granulomaMercury granulomaSilica granulomaSilicone granulomaZirconium granulomaSoot tattooTattooCarbon staineosinophilic dermatosisGranuloma facialeDermisCutaneous lupuserythematosusDiscoidPanniculitissubacuteNeonatalChilblainLupus erythematosus–lichen planus overlap syndromeVerrucousRowell's syndromeSclerodermaLocalized sclerodermaLocalized morpheaMorphea–lichen sclerosus et atrophicus overlapGeneralized morpheaAtrophoderma of Pasini and PieriniPansclerotic morpheaMorphea profundaLinear sclerodermaAtrophicatrophodermaLichen sclerosusAnetodermaSchweninger–Buzzi anetodermaJadassohn–Pellizzari anetodermaAcrodermatitis chronica atrophicansSemicircular lipoatrophyFollicular atrophodermaLinear atrophoderma of MoulinAtrophia maculosa varioliformis cutisKyrle diseaseReactive perforating collagenosisElastosis perforans serpiginosaPerforating folliculitisAcquired perforating dermatosisSkin ulcerPyoderma gangrenosumCalcinosis cutisPoikiloderma vasculare atrophicansAinhumPseudo-ainhum