Differentials: Mal De Meleda

Differential diagnosis for Mal De Meleda

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This list is calculated based on an algorithm and may be inaccurate. Google search based on different algorithm is also displayed. Please interpret with caution. Click here to search for differential diagnosis for a set of clinical findings or a short case summary. The images are provided by Bing Image Search. The images may not be related to Mal De Meleda.

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Date Added: 2018-03-16:

Palmoplantar Keratoderma (57 %)
Vohwinkel Syndrome (51 %) ( Keratoderma Hereditaria Mutilans, Keratoma Hereditaria Mutilans, Mutilating Keratoderma Of Vohwinkel, Mutilating Palmoplantar Keratoderma,)
Amniotic Band Syndrome (43 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Ehlers danlos Syndrome (43 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Olmsted Syndrome (38 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Ainhum (38 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Palmoplantar Pustulosis (37 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Clubbing (37 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Dyshidrosis (35 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Epidermolytic Hyperkeratosis (35 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Knuckle Pads (34 %) ( Heloderma,)
Heloderma (34 %) ( Knuckle Pads,)
Fissured Tongue (32 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Kindler Syndrome (32 %) ( Acrokeratotic Poikiloderma, Bullous Acrokeratotic Poikiloderma Of Kindler And Weary, Congenital Poikiloderma With Blisters And Keratoses, Congenital Poikiloderma With Bullae And Progressive Cutaneous Atrophy, Hereditary Acrokeratotic Poikiloderma, Hyperkeratosis hyperpigmentation Syndrome, Weary kindler Syndrome,)
Acrokeratosis Verruciformis (31 %) ( Acrokeratosis Verruciformis Of Hopf,)
Acrokeratosis Verruciformis Of Hopf (31 %) ( Acrokeratosis Verruciformis,)
Pachyonychia Congenita (29 %)
Follicular Mucinosis (29 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Keratitis ichthyosis deafness Syndrome (29 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Porokeratosis (29 %)
Lichenoid Keratosis (29 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Nevus Sebaceous (29 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Punctate Palmoplantar Keratoderma (29 %)
Woolly Hair (28 %) ( Wooly Hair,)
Steatocystoma Multiplex (28 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Pachydermoperiostosis (28 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Wooly Hair (28 %) ( Woolly Hair,)
Dermatopathia Pigmentosa Reticularis (28 %) ( Dermatopathia Pigmentosa Reticularis Hyperkeratotica Et Mutilans, Dermatopathia Pigmentosa Reticularis Hypohidotica Et Atrophica, Dermatopathic Pigmentosa Reticularis,)
Peeling Skin Syndrome (28 %) ( Acral Peeling Skin Syndrome, Continual Peeling Skin Syndrome, Familial Continual Skin Peeling, Idiopathic Deciduous Skin, Keratolysis Exfoliativa Congenita,)
Pagetoid Reticulosis (28 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Hidrotic Ectodermal Dysplasia (28 %) ( Alopecia Congenita With Keratosis Palmoplantaris, Clouston Syndrome, Cloustons Hidrotic Ectodermal Dysplasia, Fischer jacobsen clouston Syndrome, Keratosis Palmaris With Drumstick Fingers, Palmoplantar Keratoderma And Clubbing,)
Epidermolysis Bullosa Simplex With Mottled Pigmentation (28 %)
Conradi h nermann Syndrome (26 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Ichthyosis Bullosa Of Siemens (26 %) ( Ichthyosis Exfoliativa,)
Ichthyosis Exfoliativa (26 %) ( Ichthyosis Bullosa Of Siemens,)
Erythrokeratodermia Progressiva Symmetrica (26 %) ( Progressive Symmetric Erythrokeratodermia,)
Progressive Symmetric Erythrokeratodermia (26 %) ( Erythrokeratodermia Progressiva Symmetrica,)
Tyrosinemia Type Ii (26 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Leukonychia (26 %) ( White Nails,)
White Nails (26 %) ( Leukonychia,)
Pseudo-ainhum (26 %)
Anetoderma (26 %) ( Anetoderma Maculosa, Anetoderma Maculosa Cutis, Atrophia Maculosa Cutis, Macular Atrophy,)
Cutis Laxa (26 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Dermatitis Repens (26 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Dyschromatosis Universalis Hereditaria (26 %)
Aquagenic Keratoderma (26 %) ( Acquired Aquagenic Palmoplantar Keratoderma, Aquagenic Syringeal Acrokeratoderma, Aquagenic Wrinkling Of The Palms, Transient Reactive Papulotranslucent Acrokeratoderma,)
Keratoelastoidosis Marginalis (26 %) ( Acrokeratoelastoidosis Of Costa,)
Focal Acral Hyperkeratosis (26 %) ( Acrokeratoelastoidosis Lichenoides, Degenerative Collagenous Plaques Of The Hand,)
Anhidrosis (26 %) ( Hypohidrosis,)
Monilethrix (26 %) ( Beaded Hair,)
Acrokeratoelastoidosis Of Costa (26 %) ( Keratoelastoidosis Marginalis,)
Hypohidrosis (26 %) ( Anhidrosis,)
Beaded Hair (26 %) ( Monilethrix,)
Palmoplantar Hyperhidrosis (25 %) ( Emotional Hyperhidrosis,)
Tripe Palms (25 %)
Acrokeratoelastoidosis (25 %)
Acute Febrile Neutrophilic Dermatosis (25 %) ( Sweets Syndrome,)
Skin Fragility Syndrome (25 %) ( Plakophilin1 Deficiency,)
Emotional Hyperhidrosis (25 %) ( Palmoplantar Hyperhidrosis,)
Plakophilin1 Deficiency (25 %) ( Skin Fragility Syndrome,)
Lichen Planus Verrucosus (25 %) ( Hypertrophic Lichen Planus,)
Hypertrophic Lichen Planus (25 %) ( Lichen Planus Verrucosus,)
Clear Cell Acanthoma (25 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Keratosis Pilaris (25 %)
Smooth Tongue (25 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Ichthyosis Vulgaris (25 %) ( Autosomal Dominant Ichthyosis, Ichthyosis Simplex,)
Chromatophore Nevus Of Naegeli (23 %) ( Naegeli franceschetti jadassohn Syndrome,)
Verrucous Lupus Erythematosus (23 %) ( Hypertrophic Lupus Erythematosus,)
Naegeli-franceschetti-jadassohn Syndrome (23 %)
Hypertrophic Lupus Erythematosus (23 %) ( Verrucous Lupus Erythematosus,)
Erythema Induratum (23 %) ( Bazin Disease, Nodular Vasculitis,)
Naegeli franceschetti jadassohn Syndrome (23 %) ( Chromatophore Nevus Of Naegeli,)
Plaque-type Porokeratosis (23 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Porokeratosis Plantaris Discreta (23 %)
Sweets Syndrome (23 %) ( Acute Febrile Neutrophilic Dermatosis,)
Dystrophic Epidermolysis Bullosa (23 %)
Linear Verrucous Epidermal Nevus (23 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Lupus Erythematosus Panniculitis (23 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Lichen Planopilaris (23 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Seborrheic Keratosis (23 %) ( Seborrheic Verruca, Senile Wart,)
Noncicatricial Alopecia (23 %)
Callus (23 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Onychorrhexis (23 %) ( Brittle Nails,)
Brittle Nails (23 %) ( Onychorrhexis,)
Ichthyosis Follicularis With Alopecia And Photophobia Syndrome (22 %) ( Ichthyosis Follicularis,)
Spoon Nails (22 %) ( Koilonychia,)
Congenital Ichthyosiform Erythroderma (22 %) ( Nonbullous Congenital Ichthyosiform Erythroderma,)
Atrophodermia Vermiculata (22 %) ( Acne Vermoulante, Acne Vermoulanti, Atrophoderma Reticulata Symmetrica Faciei, Atrophoderma Reticulatum, Atrophoderma Vermiculata, Atrophoderma Vermiculatum, Atrophodermia Reticulata Symmetrica Faciei, Atrophodermia Ulerythematosa, Atrophodermie Vermicul e Des Joues AvecK ratoses Folliculaires, Folliculitis Ulerythema Reticulata, Folliculitis Ulerythematous Reticulata, Folliculitis Ulerythemosa, Honeycomb Atrophy, Ulerythema Acneforme, Ulerythema Acneiforme,)
Cicatricial Pemphigoid (22 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Keratolytic Winter Erythema (22 %) ( Erythrokeratolysis Hiemalis, Oudtshoorn Disease, Oudtshoorn Skin,)
Ichthyosis Follicularis (22 %) ( Ichthyosis Follicularis With Alopecia And Photophobia Syndrome,)
Junctional Epidermolysis Bullosa Gravis (22 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Cutaneous Lymphoid Hyperplasia (22 %) ( Borrelial Lymphocytoma, Lymphadenosis Benigna Cutis, Lymphocytoma Cutis, Pseudolymphoma, Pseudolymphoma Of Spiegler And Fendt, Sarcoidosis Of Spiegler And Fendt, Spiegler fendt Lymphoid Hyperplasia, Spiegler fendt Sarcoid,)
Lethal Acantholytic Epidermolysis Bullosa (22 %)
Papular Mucinosis (22 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Collodion Baby (22 %) ( Lamellar Ichthyosis,)
Factitious Dermatitis (22 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Acquired Ichthyosis (22 %) ( Ichthyosis Acquisita,)
Pili Torti (22 %) ( Twisted Hairs,)
Keratoderma Climactericum (22 %) ( Acquired Plantar Keratoderma, Climacteric Keratoderma, Haxthausens Disease,)
Acroosteolysis (22 %)
Twisted Hairs (22 %) ( Pili Torti,)
Epidermal Cyst (22 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Palmoplantar Erythrodysesthesia Syndrome (22 %) ( Chemotherapy-induced Acral Erythema,)
Alopecia Areata (22 %)
Oculodentodigital Dysplasia (22 %)
Epidermolysis Bullosa Simplex (22 %)
Koilonychia (22 %) ( Spoon Nails,)
Nonbullous Congenital Ichthyosiform Erythroderma (22 %) ( Congenital Ichthyosiform Erythroderma,)
Multiple Lentigines Syndrome (22 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Lichen Nitidus (22 %)
Papillon lef vre Syndrome (22 %) ( Palmoplantar Keratoderma With Periodontitis,)
Chemotherapy-induced Acral Erythema (22 %) ( Palmoplantar Erythrodysesthesia Syndrome,)
Ichthyosis Acquisita (22 %) ( Acquired Ichthyosis,)
Lamellar Ichthyosis (22 %) ( Collodion Baby,)
Oral Lichen Planus (22 %)
Trichorrhexis Invaginata (22 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Nevus Flammeus (22 %) ( Capillary Malformation, Port-wine Stain,)
Dermatofibroma (20 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Hamartoma (20 %)
Angiolymphoid Hyperplasia With Eosinophilia (20 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Popsicle Panniculitis (20 %) ( Cold Panniculitis,)
Cold Panniculitis (20 %) ( Popsicle Panniculitis,)
Lupus Erythematosus lichen Planus Overlap Syndrome (20 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Acute Generalized Exanthematous Pustulosis (20 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Lichen Planus lupus Erythematosus Overlap Syndrome (20 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Carney Complex (20 %) ( Lamb Syndrome, Name Syndrome,)
X-linked Ichthyosis (20 %) ( Steroid Sulfatase Deficiency, X-linked Recessive Ichthyosis,)
Hypohidrotic Ectodermal Dysplasia (20 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Dysplastic Nevus (20 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Carvajal Syndrome (20 %) ( Striate Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Striate Palmoplantar Keratoderma With Woolly Hair And Left Ventricular Dilated Cardiomyopathy,)
Palmoplantar Keratoderma With Periodontitis (20 %) ( Papillon lef vre Syndrome,)
Chilblains (20 %) ( Pernio, Perniosis,)
Fabry Disease (20 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Lichen Myxedematosus (20 %)
Glomus Tumor (20 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Onychogryphosis (20 %) ( Rams Horn Nails,)
Anonychia (20 %)
Perforating Folliculitis (20 %)
Diabetic Dermopathy (20 %) ( Shin Spots,)
Shin Spots (20 %) ( Diabetic Dermopathy,)
Pemphigus Vulgaris (20 %)
Id Reaction (20 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Rams Horn Nails (20 %) ( Onychogryphosis,)
Irritated Seborrheic Keratosis (20 %) ( Basosquamous Cell Acanthoma, Inflamed Seborrheic Keratosis,)
Follicular Atrophoderma (20 %)
Acrochordon (20 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Hidradenitis Suppurativa (20 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Acrospiroma (20 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Wrinkly Skin Syndrome (20 %)
Erythema Gyratum Repens (20 %) ( Gammels Disease,)
Aplasia Cutis Congenita (20 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Gammels Disease (20 %) ( Erythema Gyratum Repens,)
Harlequin-type Ichthyosis (20 %) ( Harlequin Baby, Harlequin Fetus, Harlequin Ichthyosis, Ichthyosis Congenita, Ichthyosis Congenita Gravior,)
Psoriasis Vulgaris (20 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)

Differentials from Google.

Date Added: 2018-02-16


Mal De Meleda
Palmoplantar Keratoderma

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