Differentials: Mal De Meleda

Differential diagnosis for Mal De Meleda

( DermDifferential - Drag this link to bookmarks bar for instant search)

Skin Deep - A Dermatology Blog

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.

Searching........Please wait.

Date Added: 2017-09-14:

Palmoplantar Keratoderma (56 %)
Vohwinkel Syndrome (50 %) ( Keratoderma Hereditaria Mutilans, Keratoma Hereditaria Mutilans, Mutilating Keratoderma Of Vohwinkel, Mutilating Palmoplantar Keratoderma,)
Ehlers danlos Syndrome (42 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Amniotic Band Syndrome (42 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
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 (38 %) ( 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 (36 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Clubbing (34 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Heloderma (33 %) ( Knuckle Pads,)
Knuckle Pads (33 %) ( Heloderma,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Kindler Syndrome (33 %) ( 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,)
Dyshidrosis (33 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Acrokeratosis Verruciformis (31 %) ( Acrokeratosis Verruciformis Of Hopf,)
Acrokeratosis Verruciformis Of Hopf (31 %) ( Acrokeratosis Verruciformis,)
Keratitis ichthyosis deafness Syndrome (30 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Follicular Mucinosis (30 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Nevus Sebaceous (30 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Pachyonychia Congenita (30 %)
Lichenoid Keratosis (30 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Wooly Hair (28 %) ( Woolly Hair,)
Woolly Hair (28 %) ( Wooly Hair,)
Epidermolysis Bullosa Simplex With Mottled Pigmentation (28 %)
Punctate Palmoplantar Keratoderma (28 %)
Steatocystoma Multiplex (28 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Porokeratosis (28 %)
Pagetoid Reticulosis (28 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Peeling Skin Syndrome (28 %) ( Acral Peeling Skin Syndrome, Continual Peeling Skin Syndrome, Familial Continual Skin Peeling, Idiopathic Deciduous Skin, Keratolysis Exfoliativa Congenita,)
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,)
Dermatopathia Pigmentosa Reticularis (28 %) ( Dermatopathia Pigmentosa Reticularis Hyperkeratotica Et Mutilans, Dermatopathia Pigmentosa Reticularis Hypohidotica Et Atrophica, Dermatopathic Pigmentosa Reticularis,)
Anetoderma (27 %) ( Anetoderma Maculosa, Anetoderma Maculosa Cutis, Atrophia Maculosa Cutis, Macular Atrophy,)
Dyschromatosis Universalis Hereditaria (27 %)
Keratoelastoidosis Marginalis (27 %) ( Acrokeratoelastoidosis Of Costa,)
Progressive Symmetric Erythrokeratodermia (27 %) ( Erythrokeratodermia Progressiva Symmetrica,)
Erythrokeratodermia Progressiva Symmetrica (27 %) ( Progressive Symmetric Erythrokeratodermia,)
Tyrosinemia Type Ii (27 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Cutis Laxa (27 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Leukonychia (27 %) ( White Nails,)
White Nails (27 %) ( Leukonychia,)
Ichthyosis Exfoliativa (27 %) ( Ichthyosis Bullosa Of Siemens,)
Focal Acral Hyperkeratosis (27 %) ( Acrokeratoelastoidosis Lichenoides, Degenerative Collagenous Plaques Of The Hand,)
Conradi h nermann Syndrome (27 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Ichthyosis Bullosa Of Siemens (27 %) ( Ichthyosis Exfoliativa,)
Monilethrix (27 %) ( Beaded Hair,)
Anhidrosis (27 %) ( Hypohidrosis,)
Hypohidrosis (27 %) ( Anhidrosis,)
Acrokeratoelastoidosis Of Costa (27 %) ( Keratoelastoidosis Marginalis,)
Beaded Hair (27 %) ( Monilethrix,)
Skin Fragility Syndrome (25 %) ( Plakophilin1 Deficiency,)
Keratosis Pilaris (25 %)
Tripe Palms (25 %)
Acute Febrile Neutrophilic Dermatosis (25 %) ( Sweets Syndrome,)
Hypertrophic Lichen Planus (25 %) ( Lichen Planus Verrucosus,)
Plakophilin1 Deficiency (25 %) ( Skin Fragility Syndrome,)
Ichthyosis Vulgaris (25 %) ( Autosomal Dominant Ichthyosis, Ichthyosis Simplex,)
Aquagenic Keratoderma (25 %) ( Acquired Aquagenic Palmoplantar Keratoderma, Aquagenic Syringeal Acrokeratoderma, Aquagenic Wrinkling Of The Palms, Transient Reactive Papulotranslucent Acrokeratoderma,)
Acrokeratoelastoidosis (25 %)
Smooth Tongue (25 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Pachydermoperiostosis (25 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Lichen Planus Verrucosus (25 %) ( Hypertrophic Lichen Planus,)
Pseudo-ainhum (25 %)
Naegeli franceschetti jadassohn Syndrome (23 %) ( Chromatophore Nevus Of Naegeli,)
Porokeratosis Plantaris Discreta (23 %)
Linear Verrucous Epidermal Nevus (23 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Dermatitis Repens (23 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Noncicatricial Alopecia (23 %)
Sweets Syndrome (23 %) ( Acute Febrile Neutrophilic Dermatosis,)
Lupus Erythematosus Panniculitis (23 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Dystrophic Epidermolysis Bullosa (23 %)
Naegeli-franceschetti-jadassohn Syndrome (23 %)
Lichen Planopilaris (23 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Emotional Hyperhidrosis (23 %) ( Palmoplantar Hyperhidrosis,)
Chromatophore Nevus Of Naegeli (23 %) ( Naegeli franceschetti jadassohn Syndrome,)
Callus (23 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Verrucous Lupus Erythematosus (23 %) ( Hypertrophic Lupus Erythematosus,)
Palmoplantar Hyperhidrosis (23 %) ( Emotional Hyperhidrosis,)
Clear Cell Acanthoma (23 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Hypertrophic Lupus Erythematosus (23 %) ( Verrucous Lupus Erythematosus,)
Lichen Nitidus (22 %)
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,)
Brittle Nails (22 %) ( Onychorrhexis,)
Onychorrhexis (22 %) ( Brittle Nails,)
Lamellar Ichthyosis (22 %) ( Collodion Baby,)
Palmoplantar Erythrodysesthesia Syndrome (22 %) ( Chemotherapy-induced Acral Erythema,)
Ichthyosis Follicularis With Alopecia And Photophobia Syndrome (22 %) ( Ichthyosis Follicularis,)
Alopecia Areata (22 %)
Erythema Induratum (22 %) ( Bazin Disease, Nodular Vasculitis,)
Papillon lef vre Syndrome (22 %) ( Palmoplantar Keratoderma With Periodontitis,)
Acquired Ichthyosis (22 %) ( Ichthyosis Acquisita,)
Lethal Acantholytic Epidermolysis Bullosa (22 %)
Oral Lichen Planus (22 %)
Twisted Hairs (22 %) ( Pili Torti,)
Congenital Ichthyosiform Erythroderma (22 %) ( Nonbullous Congenital Ichthyosiform Erythroderma,)
Collodion Baby (22 %) ( Lamellar Ichthyosis,)
Keratolytic Winter Erythema (22 %) ( Erythrokeratolysis Hiemalis, Oudtshoorn Disease, Oudtshoorn Skin,)
Ichthyosis Follicularis (22 %) ( Ichthyosis Follicularis With Alopecia And Photophobia Syndrome,)
Pili Torti (22 %) ( Twisted Hairs,)
Ichthyosis Acquisita (22 %) ( Acquired Ichthyosis,)
Junctional Epidermolysis Bullosa Gravis (22 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Plaque-type Porokeratosis (22 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Chemotherapy-induced Acral Erythema (22 %) ( Palmoplantar Erythrodysesthesia Syndrome,)
Cicatricial Pemphigoid (22 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
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,)
Oculodentodigital Dysplasia (22 %)
Seborrheic Keratosis (22 %) ( Seborrheic Verruca, Senile Wart,)
Trichorrhexis Invaginata (22 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Papular Mucinosis (22 %) ( Generalized Lichen Myxedematosus, Sclerodermoid Lichen Myxedematosus, Scleromyxedema,)
Epidermolysis Bullosa Simplex (22 %)
Hidradenitis Suppurativa (20 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Keratoderma Climactericum (20 %) ( Acquired Plantar Keratoderma, Climacteric Keratoderma, Haxthausens Disease,)
Pemphigus Vulgaris (20 %)
Erythema Gyratum Repens (20 %) ( Gammels Disease,)
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,)
Harlequin-type Ichthyosis (20 %) ( Harlequin Baby, Harlequin Fetus, Harlequin Ichthyosis, Ichthyosis Congenita, Ichthyosis Congenita Gravior,)
Hypohidrotic Ectodermal Dysplasia (20 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Acrospiroma (20 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Id Reaction (20 %) ( Disseminated Eczema, Generalized Eczema, Autoeczematization,)
X-linked Ichthyosis (20 %) ( Steroid Sulfatase Deficiency, X-linked Recessive Ichthyosis,)
Acroosteolysis (20 %)
Nevus Flammeus (20 %) ( Capillary Malformation, Port-wine Stain,)
Gammels Disease (20 %) ( Erythema Gyratum Repens,)
Lichen Myxedematosus (20 %)
Wrinkly Skin Syndrome (20 %)
Psoriasis Vulgaris (20 %) ( Chronic Stationary Psoriasis, Plaque-like Psoriasis,)
Aplasia Cutis Congenita (20 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Acute Generalized Exanthematous Pustulosis (20 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Acrochordon (20 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
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,)
Factitious Dermatitis (20 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Perforating Folliculitis (20 %)
Palmoplantar Keratoderma With Periodontitis (20 %) ( Papillon lef vre Syndrome,)
Irritated Seborrheic Keratosis (20 %) ( Basosquamous Cell Acanthoma, Inflamed Seborrheic Keratosis,)
Follicular Atrophoderma (20 %)

Differentials from Google.

From Cache (Web service failed):

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

comments powered by Disqus

|


This is an experimental application for healthcare professionals. The information presented here is not intended to diagnose, treat, cure or prevent any disease. Read disclaimer.

SkinHelpDesk.com - Evidence based skincare free

About Me

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.

Address

Bell Raj Eapen
Hamilton, ON
Canada