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: 2017-12-14:

Palmoplantar Keratoderma (55 %)
Vohwinkel Syndrome (51 %) ( Keratoderma Hereditaria Mutilans, Keratoma Hereditaria Mutilans, Mutilating Keratoderma Of Vohwinkel, Mutilating Palmoplantar Keratoderma,)
Ehlers danlos Syndrome (43 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Amniotic Band Syndrome (43 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
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 (35 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Epidermolytic Hyperkeratosis (35 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Dyshidrosis (34 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Heloderma (34 %) ( Knuckle Pads,)
Knuckle Pads (34 %) ( 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,)
Fissured Tongue (32 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Acrokeratosis Verruciformis Of Hopf (31 %) ( Acrokeratosis Verruciformis,)
Acrokeratosis Verruciformis (31 %) ( Acrokeratosis Verruciformis Of Hopf,)
Keratitis ichthyosis deafness Syndrome (29 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Punctate Palmoplantar Keratoderma (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,)
Porokeratosis (29 %)
Follicular Mucinosis (29 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Pachyonychia Congenita (29 %)
Woolly Hair (28 %) ( Wooly Hair,)
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,)
Wooly Hair (28 %) ( Woolly Hair,)
Dermatopathia Pigmentosa Reticularis (28 %) ( Dermatopathia Pigmentosa Reticularis Hyperkeratotica Et Mutilans, Dermatopathia Pigmentosa Reticularis Hypohidotica Et Atrophica, Dermatopathic Pigmentosa Reticularis,)
Epidermolysis Bullosa Simplex With Mottled Pigmentation (28 %)
Peeling Skin Syndrome (28 %) ( Acral Peeling Skin Syndrome, Continual Peeling Skin Syndrome, Familial Continual Skin Peeling, Idiopathic Deciduous Skin, Keratolysis Exfoliativa Congenita,)
Steatocystoma Multiplex (28 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Anetoderma (26 %) ( Anetoderma Maculosa, Anetoderma Maculosa Cutis, Atrophia Maculosa Cutis, Macular Atrophy,)
Monilethrix (26 %) ( Beaded Hair,)
Aquagenic Keratoderma (26 %) ( Acquired Aquagenic Palmoplantar Keratoderma, Aquagenic Syringeal Acrokeratoderma, Aquagenic Wrinkling Of The Palms, Transient Reactive Papulotranslucent Acrokeratoderma,)
Focal Acral Hyperkeratosis (26 %) ( Acrokeratoelastoidosis Lichenoides, Degenerative Collagenous Plaques Of The Hand,)
Acrokeratoelastoidosis Of Costa (26 %) ( Keratoelastoidosis Marginalis,)
Erythrokeratodermia Progressiva Symmetrica (26 %) ( Progressive Symmetric Erythrokeratodermia,)
Tyrosinemia Type Ii (26 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Keratoelastoidosis Marginalis (26 %) ( Acrokeratoelastoidosis Of Costa,)
Progressive Symmetric Erythrokeratodermia (26 %) ( Erythrokeratodermia Progressiva Symmetrica,)
Anhidrosis (26 %) ( Hypohidrosis,)
Ichthyosis Bullosa Of Siemens (26 %) ( Ichthyosis Exfoliativa,)
Ichthyosis Exfoliativa (26 %) ( Ichthyosis Bullosa Of Siemens,)
White Nails (26 %) ( Leukonychia,)
Dyschromatosis Universalis Hereditaria (26 %)
Leukonychia (26 %) ( White Nails,)
Pseudo-ainhum (26 %)
Hypohidrosis (26 %) ( Anhidrosis,)
Beaded Hair (26 %) ( Monilethrix,)
Pachydermoperiostosis (26 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Cutis Laxa (26 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Conradi h nermann Syndrome (26 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Plakophilin1 Deficiency (25 %) ( Skin Fragility Syndrome,)
Keratosis Pilaris (25 %)
Smooth Tongue (25 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Hypertrophic Lichen Planus (25 %) ( Lichen Planus Verrucosus,)
Tripe Palms (25 %)
Skin Fragility Syndrome (25 %) ( Plakophilin1 Deficiency,)
Acute Febrile Neutrophilic Dermatosis (25 %) ( Sweets Syndrome,)
Dermatitis Repens (25 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Acrokeratoelastoidosis (25 %)
Lichen Planus Verrucosus (25 %) ( Hypertrophic Lichen Planus,)
Ichthyosis Vulgaris (25 %) ( Autosomal Dominant Ichthyosis, Ichthyosis Simplex,)
Hypertrophic Lupus Erythematosus (23 %) ( Verrucous Lupus Erythematosus,)
Porokeratosis Plantaris Discreta (23 %)
Lichen Planopilaris (23 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Chromatophore Nevus Of Naegeli (23 %) ( Naegeli franceschetti jadassohn Syndrome,)
Emotional Hyperhidrosis (23 %) ( Palmoplantar Hyperhidrosis,)
Dystrophic Epidermolysis Bullosa (23 %)
Palmoplantar Hyperhidrosis (23 %) ( Emotional Hyperhidrosis,)
Naegeli franceschetti jadassohn Syndrome (23 %) ( Chromatophore Nevus Of Naegeli,)
Onychorrhexis (23 %) ( Brittle Nails,)
Erythema Induratum (23 %) ( Bazin Disease, Nodular Vasculitis,)
Callus (23 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Sweets Syndrome (23 %) ( Acute Febrile Neutrophilic Dermatosis,)
Brittle Nails (23 %) ( Onychorrhexis,)
Clear Cell Acanthoma (23 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Verrucous Lupus Erythematosus (23 %) ( Hypertrophic Lupus Erythematosus,)
Naegeli-franceschetti-jadassohn Syndrome (23 %)
Noncicatricial Alopecia (23 %)
Plaque-type Porokeratosis (23 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
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,)
Ichthyosis Acquisita (22 %) ( Acquired Ichthyosis,)
Cicatricial Pemphigoid (22 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Acroosteolysis (22 %)
Lethal Acantholytic Epidermolysis Bullosa (22 %)
Pili Torti (22 %) ( Twisted Hairs,)
Oculodentodigital Dysplasia (22 %)
Twisted Hairs (22 %) ( Pili Torti,)
Congenital Ichthyosiform Erythroderma (22 %) ( Nonbullous Congenital Ichthyosiform Erythroderma,)
Oral Lichen Planus (22 %)
Acquired Ichthyosis (22 %) ( Ichthyosis Acquisita,)
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,)
Palmoplantar Erythrodysesthesia Syndrome (22 %) ( Chemotherapy-induced Acral Erythema,)
Keratolytic Winter Erythema (22 %) ( Erythrokeratolysis Hiemalis, Oudtshoorn Disease, Oudtshoorn Skin,)
Seborrheic Keratosis (22 %) ( Seborrheic Verruca, Senile Wart,)
Junctional Epidermolysis Bullosa Gravis (22 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Trichorrhexis Invaginata (22 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Lichen Nitidus (22 %)
Papillon lef vre Syndrome (22 %) ( Palmoplantar Keratoderma With Periodontitis,)
Ichthyosis Follicularis (22 %) ( Ichthyosis Follicularis With Alopecia And Photophobia Syndrome,)
Alopecia Areata (22 %)
Chemotherapy-induced Acral Erythema (22 %) ( Palmoplantar Erythrodysesthesia Syndrome,)
Epidermolysis Bullosa Simplex (22 %)
Collodion Baby (22 %) ( Lamellar Ichthyosis,)
Ichthyosis Follicularis With Alopecia And Photophobia Syndrome (22 %) ( Ichthyosis Follicularis,)
Lamellar Ichthyosis (22 %) ( Collodion Baby,)
Nonbullous Congenital Ichthyosiform Erythroderma (22 %) ( Congenital Ichthyosiform Erythroderma,)
Papular Mucinosis (22 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Multiple Lentigines Syndrome (22 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Hypohidrotic Ectodermal Dysplasia (20 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Harlequin-type Ichthyosis (20 %) ( Harlequin Baby, Harlequin Fetus, Harlequin Ichthyosis, Ichthyosis Congenita, Ichthyosis Congenita Gravior,)
Follicular Atrophoderma (20 %)
Perforating Folliculitis (20 %)
Epidermal Cyst (20 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Carvajal Syndrome (20 %) ( Striate Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Striate Palmoplantar Keratoderma With Woolly Hair And Left Ventricular Dilated Cardiomyopathy,)
Koilonychia (20 %) ( Spoon Nails,)
Chilblains (20 %) ( Pernio, Perniosis,)
Keratoderma Climactericum (20 %) ( Acquired Plantar Keratoderma, Climacteric Keratoderma, Haxthausens Disease,)
Id Reaction (20 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
Palmoplantar Keratoderma With Periodontitis (20 %) ( Papillon lef vre Syndrome,)
Pemphigus Vulgaris (20 %)
Spoon Nails (20 %) ( Koilonychia,)
Dysplastic Nevus (20 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
X-linked Ichthyosis (20 %) ( Steroid Sulfatase Deficiency, X-linked Recessive Ichthyosis,)
Gammels Disease (20 %) ( Erythema Gyratum Repens,)
Erythema Gyratum Repens (20 %) ( Gammels Disease,)
Lichen Myxedematosus (20 %)
Factitious Dermatitis (20 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Lupus Erythematosus lichen Planus Overlap Syndrome (20 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Irritated Seborrheic Keratosis (20 %) ( Basosquamous Cell Acanthoma, Inflamed Seborrheic Keratosis,)
Atrophodermia Vermiculata (20 %) ( 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,)
Popsicle Panniculitis (20 %) ( Cold Panniculitis,)
Cold Panniculitis (20 %) ( Popsicle Panniculitis,)
Acute Generalized Exanthematous Pustulosis (20 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Rams Horn Nails (20 %) ( Onychogryphosis,)
Onychogryphosis (20 %) ( Rams Horn Nails,)
Aplasia Cutis Congenita (20 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Wrinkly Skin Syndrome (20 %)
Acrospiroma (20 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Psoriasis Vulgaris (20 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Nevus Flammeus (20 %) ( Capillary Malformation, Port-wine Stain,)
Anonychia (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,)
Lichen Planus lupus Erythematosus Overlap Syndrome (20 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)

Differentials from Google.

Date Added: 2018-02-16


Mal De Meleda
Palmoplantar Keratoderma

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I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.

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