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: 2017-03-16:

Palmoplantar Keratoderma (56 %)
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 (41 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Ainhum (38 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Olmsted Syndrome (38 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
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,)
Epidermolytic Hyperkeratosis (35 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Clubbing (35 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Dyshidrosis (33 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Heloderma (32 %) ( Knuckle Pads,)
Knuckle Pads (32 %) ( Heloderma,)
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 Of Hopf (32 %) ( Acrokeratosis Verruciformis,)
Acrokeratosis Verruciformis (32 %) ( Acrokeratosis Verruciformis Of Hopf,)
Pachyonychia Congenita (30 %)
Woolly Hair (29 %) ( Wooly Hair,)
Nevus Sebaceous (29 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Peeling Skin Syndrome (29 %) ( Acral Peeling Skin Syndrome, Continual Peeling Skin Syndrome, Familial Continual Skin Peeling, Idiopathic Deciduous Skin, Keratolysis Exfoliativa Congenita,)
Epidermolysis Bullosa Simplex With Mottled Pigmentation (29 %)
Hidrotic Ectodermal Dysplasia (29 %) ( Alopecia Congenita With Keratosis Palmoplantaris, Clouston Syndrome, Cloustons Hidrotic Ectodermal Dysplasia, Fischer jacobsen clouston Syndrome, Keratosis Palmaris With Drumstick Fingers, Palmoplantar Keratoderma And Clubbing,)
Lichenoid Keratosis (29 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Keratitis ichthyosis deafness Syndrome (29 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Wooly Hair (29 %) ( Woolly Hair,)
Follicular Mucinosis (29 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Ichthyosis Exfoliativa (27 %) ( Ichthyosis Bullosa Of Siemens,)
Ichthyosis Bullosa Of Siemens (27 %) ( Ichthyosis Exfoliativa,)
Erythrokeratodermia Progressiva Symmetrica (27 %) ( Progressive Symmetric Erythrokeratodermia,)
Progressive Symmetric Erythrokeratodermia (27 %) ( Erythrokeratodermia Progressiva Symmetrica,)
Porokeratosis (27 %)
Punctate Palmoplantar Keratoderma (27 %)
Tyrosinemia Type Ii (27 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Leukonychia (27 %) ( White Nails,)
Dermatopathia Pigmentosa Reticularis (27 %) ( Dermatopathia Pigmentosa Reticularis Hyperkeratotica Et Mutilans, Dermatopathia Pigmentosa Reticularis Hypohidotica Et Atrophica, Dermatopathic Pigmentosa Reticularis,)
White Nails (27 %) ( Leukonychia,)
Steatocystoma Multiplex (27 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Keratoelastoidosis Marginalis (27 %) ( Acrokeratoelastoidosis Of Costa,)
Anhidrosis (27 %) ( Hypohidrosis,)
Hypohidrosis (27 %) ( Anhidrosis,)
Focal Acral Hyperkeratosis (27 %) ( Acrokeratoelastoidosis Lichenoides, Degenerative Collagenous Plaques Of The Hand,)
Beaded Hair (27 %) ( Monilethrix,)
Monilethrix (27 %) ( Beaded Hair,)
Pagetoid Reticulosis (27 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Acrokeratoelastoidosis Of Costa (27 %) ( Keratoelastoidosis Marginalis,)
Keratosis Pilaris (25 %)
Anetoderma (25 %) ( Anetoderma Maculosa, Anetoderma Maculosa Cutis, Atrophia Maculosa Cutis, Macular Atrophy,)
Cutis Laxa (25 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Pseudo-ainhum (25 %)
Dyschromatosis Universalis Hereditaria (25 %)
Tripe Palms (25 %)
Conradi h nermann Syndrome (25 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Aquagenic Keratoderma (25 %) ( Acquired Aquagenic Palmoplantar Keratoderma, Aquagenic Syringeal Acrokeratoderma, Aquagenic Wrinkling Of The Palms, Transient Reactive Papulotranslucent Acrokeratoderma,)
Pachydermoperiostosis (24 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Lichen Planus Verrucosus (24 %) ( Hypertrophic Lichen Planus,)
Verrucous Lupus Erythematosus (24 %) ( Hypertrophic Lupus Erythematosus,)
Ichthyosis Vulgaris (24 %) ( Autosomal Dominant Ichthyosis, Ichthyosis Simplex,)
Dermatitis Repens (24 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Hypertrophic Lichen Planus (24 %) ( Lichen Planus Verrucosus,)
Chromatophore Nevus Of Naegeli (24 %) ( Naegeli franceschetti jadassohn Syndrome,)
Acute Febrile Neutrophilic Dermatosis (24 %) ( Sweets Syndrome,)
Acrokeratoelastoidosis (24 %)
Emotional Hyperhidrosis (24 %) ( Palmoplantar Hyperhidrosis,)
Porokeratosis Plantaris Discreta (24 %)
Naegeli franceschetti jadassohn Syndrome (24 %) ( Chromatophore Nevus Of Naegeli,)
Smooth Tongue (24 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Plakophilin1 Deficiency (24 %) ( Skin Fragility Syndrome,)
Naegeli-franceschetti-jadassohn Syndrome (24 %)
Palmoplantar Hyperhidrosis (24 %) ( Emotional Hyperhidrosis,)
Hypertrophic Lupus Erythematosus (24 %) ( Verrucous Lupus Erythematosus,)
Skin Fragility Syndrome (24 %) ( Plakophilin1 Deficiency,)
Papillon lef vre Syndrome (22 %) ( Palmoplantar Keratoderma With Periodontitis,)
Ichthyosis Acquisita (22 %) ( Acquired Ichthyosis,)
Lichen Nitidus (22 %)
Keratolytic Winter Erythema (22 %) ( Erythrokeratolysis Hiemalis, Oudtshoorn Disease, Oudtshoorn Skin,)
Ichthyosis Follicularis (22 %) ( Ichthyosis Follicularis With Alopecia And Photophobia Syndrome,)
Dystrophic Epidermolysis Bullosa (22 %)
Lichen Planopilaris (22 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Collodion Baby (22 %) ( Lamellar Ichthyosis,)
Lethal Acantholytic Epidermolysis Bullosa (22 %)
Lamellar Ichthyosis (22 %) ( Collodion Baby,)
Ichthyosis Follicularis With Alopecia And Photophobia Syndrome (22 %) ( Ichthyosis Follicularis,)
Congenital Ichthyosiform Erythroderma (22 %) ( Nonbullous Congenital Ichthyosiform Erythroderma,)
Nonbullous Congenital Ichthyosiform Erythroderma (22 %) ( Congenital Ichthyosiform Erythroderma,)
Plaque-type Porokeratosis (22 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Onychorrhexis (22 %) ( Brittle Nails,)
Brittle Nails (22 %) ( Onychorrhexis,)
Pili Torti (22 %) ( Twisted Hairs,)
Sweets Syndrome (22 %) ( Acute Febrile Neutrophilic Dermatosis,)
Clear Cell Acanthoma (22 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Linear Verrucous Epidermal Nevus (22 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Trichorrhexis Invaginata (22 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Twisted Hairs (22 %) ( Pili Torti,)
Acquired Ichthyosis (22 %) ( Ichthyosis Acquisita,)
Callus (22 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Junctional Epidermolysis Bullosa Gravis (21 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Chemotherapy-induced Acral Erythema (21 %) ( Palmoplantar Erythrodysesthesia Syndrome,)
Keratoderma Climactericum (21 %) ( Acquired Plantar Keratoderma, Climacteric Keratoderma, Haxthausens Disease,)
Papular Mucinosis (21 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Harlequin-type Ichthyosis (21 %) ( Harlequin Baby, Harlequin Fetus, Harlequin Ichthyosis, Ichthyosis Congenita, Ichthyosis Congenita Gravior,)
Cicatricial Pemphigoid (21 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Lupus Erythematosus Panniculitis (21 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Oral Lichen Planus (21 %)
Palmoplantar Erythrodysesthesia Syndrome (21 %) ( Chemotherapy-induced Acral Erythema,)
Alopecia Areata (21 %)
Factitious Dermatitis (21 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Gammels Disease (21 %) ( Erythema Gyratum Repens,)
Psoriasis Vulgaris (21 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Multiple Lentigines Syndrome (21 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Noncicatricial Alopecia (21 %)
Carvajal Syndrome (21 %) ( Striate Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Striate Palmoplantar Keratoderma With Woolly Hair And Left Ventricular Dilated Cardiomyopathy,)
Seborrheic Keratosis (21 %) ( Seborrheic Verruca, Senile Wart,)
Oculodentodigital Dysplasia (21 %)
Palmoplantar Keratoderma With Periodontitis (21 %) ( Papillon lef vre Syndrome,)
Acroosteolysis (21 %)
Erythema Gyratum Repens (21 %) ( Gammels Disease,)
Follicular Atrophoderma (21 %)
Erythema Induratum (21 %) ( Bazin Disease, Nodular Vasculitis,)
Epidermolysis Bullosa Simplex (21 %)
Cutaneous Lymphoid Hyperplasia (21 %) ( 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,)

Differentials from Google.

Date Added: 2017-03-08


Focal Acral Hyperkeratosis
Mal De Meleda
Palmoplantar Keratoderma
Porokeratosis
Porokeratosis Of Mibelli

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