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Localized granuloma annulare is a skin condition of unknown cause, tending to affect children and young to middle-aged adults, usually appearing on the lateral or dorsal surfaces of the fingers or hands, elbows, dorsal feet, and ankles.[1]:703 See also Granuloma annulare Skin lesion References ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.  This cutaneous condition article is a stub. You can help Wikipedia by expanding it. v • d • e v • d • e Cutaneous keratosis, ulcer, atrophy, and necrobiosis (L82-L94, 700-701.5) Epidermal thickening/ keratoderma/ keratosis/ hyperkeratosis PPK Inherited diffuse: Diffuse epidermolytic palmoplantar keratoderma • Diffuse nonepidermolytic palmoplantar keratoderma • Palmoplantar keratoderma of Sybert • Mal de Meleda • syndromic (connexin (Bart–Pumphrey syndrome • Clouston's hidrotic ectodermal dysplasia • Vohwinkel syndrome) • Corneodermatoosseous syndrome • plakoglobin (Naxos syndrome) • Scleroatrophic syndrome of Huriez • Olmsted syndrome • Cathepsin C (Papillon–Lefèvre syndrome • Haim–Munk syndrome) • Camisa disease focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis • Focal palmoplantar and gingival keratosis • Howel–Evans syndrome • Pachyonychia congenita (Pachyonychia congenita type I • Pachyonychia congenita type II)  • Striate palmoplantar keratoderma • Tyrosinemia type II) punctate: Acrokeratoelastoidosis of Costa • Focal acral hyperkeratosis • Keratosis punctata palmaris et plantaris • Keratosis punctata of the palmar creases • Schöpf–Schulz–Passarge syndrome • Porokeratosis plantaris discreta • Spiny keratoderma ungrouped: Palmoplantar keratoderma and spastic paraplegia • desmoplakin (Carvajal syndrome) • connexin (Erythrokeratodermia variabilis • HID/KID) Acquired Keratoderma climactericum • Paraneoplastic keratoderma • Acrokeratosis paraneoplastica of Bazex • Aquagenic keratoderma Other Acanthosis nigricans · Keloid · Seborrheic keratosis · Callus • Keratoderma blennorrhagica • Ichthyosis acquisita Skin ulcer Pyoderma gangrenosum Atrophic/atrophoderma Lichen sclerosus · Anetoderma (Schweninger–Buzzi anetoderma, Jadassohn–Pellizzari anetoderma) · Atrophoderma of Pasini and Pierini · Acrodermatitis chronica atrophicans · Semicircular lipoatrophy · Follicular atrophoderma · Linear atrophoderma of Moulin Necrobiosis/granuloma necrobiotic/palisading: Granuloma annulare (Perforating, Generalized, Subcutaneous, Granuloma annulare in HIV disease, Localized granuloma annulare, Patch-type granuloma annulare) · Necrobiosis lipoidica · Annular elastolytic giant cell granuloma · Granuloma multiforme · Necrobiotic xanthogranuloma · Palisaded neutrophilic and granulomatous dermatitis · Rheumatoid nodulosis foreign body granuloma: Silica granuloma miscellaneous/other: Granuloma faciale · Sclerosing lipogranuloma · Pyogenic granuloma · Interstitial granulomatous drug reaction · Interstitial granulomatous dermatitis Localized CTD Cutaneous lupus erythematosus chronic: Discoid · Panniculitis subacute: Neonatal ungrouped: Chilblain · Lupus erythematosus–lichen planus overlap syndrome · Tumid · Verrucous · Rowell's syndrome Scleroderma/ Morphea Localized scleroderma (Localized morphea, Morphea–lichen sclerosus et atrophicus overlap, Generalized morphea, Atrophoderma of Pasini and Pierini, Pansclerotic morphea, Morphea profunda, Linear scleroderma) Other Calcinosis cutis · Sclerodactyly · Poikiloderma vasculare atrophicans · Ainhum/Pseudo-ainhum Transepidermal elimination Kyrle disease · Reactive perforating collagenosis · Elastosis perforans serpiginosa M: INT, SF, LCT anat/phys/devp noco(i,b,d,q,u,r,p,k,c,v)/cong/tumr(n,e,d), sysi/epon proc, drug (D2/3/4/5/8)