Differentials: Witkop Syndrome

Differential diagnosis for Witkop Syndrome

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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 Witkop Syndrome.

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Date Added: 2018-04-06:

Acrocephalosyndactyly (100 %) ( Apert Syndrome,)
Lobstein Syndrome (100 %) ( Osteogenesis Imperfecta,)
Tooth And Nail Syndrome (100 %) ( Hypodontia With Nail Dysgenesis, Witkop Syndrome,)
Aplasia Cutis Congenita (100 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Maroteaux lamy Syndrome (100 %) ( Mucopolysaccharidosis Type Vi,)
Rapp hodgkin Ectodermal Dysplasia Syndrome (100 %) ( Rapp hodgkin Syndrome,)
Pyruvate Dehydrogenase Complex Deficiency (100 %)
Incontinentia Pigmenti (100 %) ( Bloch siemens Syndrome, Bloch sulzberger Disease, Bloch sulzberger Syndrome,)
Hurler Syndrome (100 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Anhidrosis (100 %) ( Hypohidrosis,)
Wooly Hair (100 %) ( Woolly Hair,)
Woolly Hair (100 %) ( Wooly Hair,)
Johanson blizzard Syndrome (100 %)
Osteogenesis Imperfecta (100 %) ( Lobstein Syndrome,)
Chondrodysplasia Punctata (100 %)
Polyostotic Fibrous Dysplasia (100 %) ( Albrights Disease,)
Neurofibromatosis Type1 (100 %) ( Von Recklinghausens Disease,)
Griscelli Syndrome Type1 (100 %) ( Elejalde Syndrome,)
Elejalde Syndrome (100 %) ( Griscelli Syndrome Type1,)
Klippel feil Syndrome (100 %)
Supernumerary Nipple (100 %) ( Accessory Nipple, Pseudomamma,)
Rhizomelic Chondrodysplasia Punctata (100 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Rapp hodgkin Syndrome (100 %) ( Rapp hodgkin Ectodermal Dysplasia Syndrome,)
Costello Syndrome (100 %)
Albrights Disease (100 %) ( Polyostotic Fibrous Dysplasia,)
Mccune albright Syndrome (100 %)
Joubert Syndrome (100 %)
Kabuki Syndrome (100 %) ( Kabuki Makeup Syndrome, Niikawa kuroki Syndrome,)
Hypohidrosis (100 %) ( Anhidrosis,)
Mckusick Type Metaphyseal Chondrodysplasia (100 %) ( Cartilage hair Hypoplasia,)
Keratitis ichthyosis deafness Syndrome (100 %) ( Erythrokeratodermia Progressiva Burns, Ichthyosiform Erythroderma With Corneal Involvement And Deafness, Kid Syndrome,)
Ectodermal Dysplasia (100 %)
Mucopolysaccharidosis Type Vi (100 %) ( Maroteaux lamy Syndrome,)
Cartilage hair Hypoplasia (100 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Von Recklinghausens Disease (100 %) ( Neurofibromatosis Type1,)
Hay wells Syndrome (100 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Ectrodactyly ectodermal Dysplasia cleft Syndrome (100 %) ( Eec Syndrome, Split Hand split Foot ectodermal Dysplasia cleft Syndrome,)
Digeorge Syndrome (100 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Apert Syndrome (100 %) ( Acrocephalosyndactyly,)
Nail patella Syndrome (100 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Langerhans Cell Histiocytosis (75 %) ( HistiocytosisX,)
Acquired Hypogammaglobulinemia (75 %) ( Common Variable Immunodeficiency,)
Common Variable Immunodeficiency (75 %) ( Acquired Hypogammaglobulinemia,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (75 %) ( Papa Syndrome,)
Lethal Acantholytic Epidermolysis Bullosa (75 %)
Marinesco sj gren Syndrome (75 %)
Marshall Syndrome (75 %)
Lhermitte duclos Disease (75 %)
Nevoid Basal Cell Carcinoma Syndrome (75 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Thrombotic Thrombocytopenic Purpura (75 %) ( Moschcowitz Syndrome,)
Familial Dysautonomia (75 %) ( Riley day Syndrome,)
Fanconi Syndrome (75 %) ( Familial Pancytopenia, Familial Panmyelophthisis,)
Hypohidrotic Ectodermal Dysplasia (75 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Hereditary Hemorrhagic Telangiectasia (75 %) ( Oslers Disease, Osler weber rendu Disease,)
Granulocytic Sarcoma (75 %) ( Chloroma, Myeloid Sarcoma,)
Hyper-ige Syndrome (75 %) ( Buckley Syndrome, Job Syndrome,)
Nevus Comedonicus Syndrome (75 %)
Multiple Endocrine Neoplasia Type3 (75 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Eosinophilic Cellulitis (75 %) ( Wells Syndrome,)
Papa Syndrome (75 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Generalized Pustular Psoriasis (75 %) ( Pustular Psoriasis Of Von Zumbusch,)
Acanthosis Nigricans Type Ii (75 %) ( Familial Acanthosis Nigricans,)
Spitz Nevus (75 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Eyelid Cysts With Palmoplantar Keratoderma And Hypodontia And Hypotrichosis (75 %) ( Sch pf schulz passarge Syndrome,)
Multiple Familial Trichoepithelioma (75 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Severe Combined Immunodeficiency (75 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome (75 %) ( Apeced Syndrome,)
Soft-tissue Melanoma (75 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Melanocytic Nevi (75 %)
Sinus Histiocytosis With Massive Lymphadenopathy (75 %) ( Rosai dorfman Disease,)
Ataxia Telangiectasia (75 %) ( Louis bar Syndrome,)
Zoster (75 %) ( Herpes Zoster, Shingles,)
Louis bar Syndrome (75 %) ( Ataxia Telangiectasia,)
Juvenile Myelomonocytic Leukemia (75 %)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (75 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Blue Nevus (75 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Recurrent Aphthous Stomatitis (75 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Tuberous Sclerosis (75 %) ( Bourneville Disease, Epiloia,)
Bannayan riley ruvalcaba Syndrome (75 %)
Kindler Syndrome (75 %) ( 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,)
Oculodentodigital Dysplasia (75 %)
Rothmund thomson Syndrome (75 %) ( Poikiloderma Congenitale,)
Infantile Myofibromatosis (75 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Sturge weber Syndrome (75 %)
Rubinstein taybi Syndrome (75 %)
Cardiofaciocutaneous Syndrome (75 %) ( Cardio-facio-cutaneous Syndrome,)
Epidermodysplasia Verruciformis (75 %)
Lymphangioma (75 %) ( Lymphangiectasis,)
Roseola Infantum (75 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Lymphangiectasis (75 %) ( Lymphangioma,)
Freckle (75 %) ( Ephelis,)
Complement Deficiency (75 %)
Wrinkly Skin Syndrome (75 %)
Ehlers danlos Syndrome (75 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Proteus Syndrome (75 %)
Phenylketonuria (75 %)
Leiomyoma (75 %)
Ehlers-danlos Syndrome (75 %)
Multiple Lentigines Syndrome (75 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Biotinidase Deficiency (75 %)
Hypoparathyroidism (75 %)
Noonan Syndrome (75 %)
Riley day Syndrome (75 %) ( Familial Dysautonomia,)
Aphthous Stomatitis (75 %)
Tricho rhino phalangeal Syndrome (75 %)
Carney Complex (75 %) ( Lamb Syndrome, Name Syndrome,)
Watson Syndrome (75 %)
Ephelis (75 %) ( Freckle,)
Peutz jeghers Syndrome (75 %)
Hunter Syndrome (75 %)
Henoch Schonlein Purpura (75 %)
Segmental Neurofibromatosis (75 %)
Niemann pick Disease (75 %)
Rosai dorfman Disease (75 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Omenn Syndrome (75 %)
Preauricular Sinus And Cyst (75 %) ( Ear Pit, Congenital Auricular Fistula, Congenital Preauricular Fistula, Preauricular Cyst,)
Limb mammary Syndrome (75 %)
Solitary Neurofibroma (75 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Nodulosis arthropathy osteolysis Syndrome (75 %)
Acquired Generalized Lipodystrophy (75 %) ( Lawrence Syndrome, Lawrence seip Syndrome,)
X-linked Lymphoproliferative Disease (75 %) ( Duncans Disease,)
Trichorrhexis Nodosa (75 %)
Beaded Hair (75 %) ( Monilethrix,)
Pili Torti (75 %) ( Twisted Hairs,)
Monilethrix (75 %) ( Beaded Hair,)
Trichorrhexis Invaginata (75 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Lowe Syndrome (75 %) ( Oculocerebrorenal Dystrophy,)
Homocystinuria (75 %)
I-cell Disease (75 %) ( Mucolipidosis Type Ii,)
Adrenoleukodystrophy (75 %) ( Schilders Disease,)
Hypophosphatasia (75 %)
Nevus Flammeus (75 %) ( Capillary Malformation, Port-wine Stain,)
Mucolipidosis Type Ii (75 %) ( I-cell Disease,)
Palmoplantar Keratoderma (75 %)
Twisted Hairs (75 %) ( Pili Torti,)
Long-chain Acyl Coa Dehydrogenase Deficiency (75 %)
Acrochordon (75 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Krabbe Disease (75 %)
Encephalocele (75 %)
Carvajal Syndrome (75 %) ( Striate Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Striate Palmoplantar Keratoderma With Woolly Hair And Left Ventricular Dilated Cardiomyopathy,)
Galactose-1-phosphate Uridyltransferase Deficiency (75 %) ( Galactosemia,)
Majeed Syndrome (75 %)
Muckle wells Syndrome (75 %)
Cyclic Neutropenia (75 %)
Popliteal Pterygium Syndrome (75 %)
Hidrotic Ectodermal Dysplasia (75 %) ( Alopecia Congenita With Keratosis Palmoplantaris, Clouston Syndrome, Cloustons Hidrotic Ectodermal Dysplasia, Fischer jacobsen clouston Syndrome, Keratosis Palmaris With Drumstick Fingers, Palmoplantar Keratoderma And Clubbing,)
Clubbing (75 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
X-linked Agammaglobulinemia (75 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Familial Cold Urticaria (75 %) ( Familial Cold Autoinflammatory Syndrome,)
Olmsted Syndrome (75 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Gingival Hypertrophy (75 %)
Leukoplakia (75 %)
Blau Syndrome (75 %)
Anonychia (75 %)
Menkes Kinky Hair Syndrome (75 %) ( Kinky Hair Disease, Menkes Disease,)
Duncans Disease (75 %) ( X-linked Lymphoproliferative Disease,)
Smooth Tongue (75 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Multiple Endocrine Neoplasia Type2 (75 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Tnf Receptor Associated Periodic Syndrome (75 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Hyper-igd Syndrome (75 %)
Familial Mediterranean Fever (75 %)
Familial Cold Autoinflammatory Syndrome (75 %) ( Familial Cold Urticaria,)
Conradi h nermann Syndrome (75 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Urticaria Pigmentosa (75 %) ( Childhood Type Of Generalized Eruption Of Cutaneous Mastocytosis,)
Fibrodysplasia Ossificans Progressiva (75 %)
Denys-drash Syndrome (75 %)
Epidermal Nevus Syndrome (75 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
De Lange Syndrome (75 %)
Juvenile Xanthogranuloma (75 %)
Wells Syndrome (75 %) ( Eosinophilic Cellulitis,)
Maple Syrup Urine Disease (75 %)
Adrenal Hyperplasia (75 %)
Familial Acanthosis Nigricans (75 %) ( Acanthosis Nigricans Type Ii,)
Sch pf schulz passarge Syndrome (75 %) ( Eyelid Cysts With Palmoplantar Keratoderma And Hypodontia And Hypotrichosis,)
Schimmelpenning Syndrome (75 %) ( Schimmelpenning feuerstein mims Syndrome,)
Schimmelpenning feuerstein mims Syndrome (75 %) ( Schimmelpenning Syndrome,)
Poikiloderma Congenitale (75 %) ( Rothmund thomson Syndrome,)
Griscelli Syndrome (75 %)
Cardio-facio-cutaneous Syndrome (75 %) ( Cardiofaciocutaneous Syndrome,)
Congenital Insensitivity To Pain With Anhidrosis (75 %)
Apeced Syndrome (75 %) ( Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome,)
Naxos Syndrome (75 %) ( Diffuse Non-epidermolytic Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Diffuse Palmoplantar Keratoderma With Woolly Hair And Arrythmogenic Right Ventricular Cardiomyopathy Of Naxos, Naxos Disease,)
X-linked Hyper-igm Syndrome (75 %)
Wiskott aldrich Syndrome (75 %)
Purine Nucleoside Phosphorylase Deficiency (75 %)
Acrodermatitis Enteropathica (75 %)
Telangiectasia (75 %)
Erythromelalgia (75 %) ( Acromelalgia, Erythermalgia,)
Dyschromatosis Symmetrica Hereditaria (75 %) ( Reticulate Acropigmentation Of Dohi, Symmetrical Dyschromatosis Of The Extremities,)
Fibrinolysis Syndrome (75 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Griscelli Syndrome Type3 (75 %)
Galactosemia (75 %) ( Galactose-1-phosphate Uridyltransferase Deficiency,)
HistiocytosisX (75 %) ( Langerhans Cell Histiocytosis,)
Gm1 Gangliosidosis (75 %)
Glycogen Storage Diseases (75 %)
Childhood Type Of Generalized Eruption Of Cutaneous Mastocytosis (75 %) ( Urticaria Pigmentosa,)
Griscelli Syndrome Type2 (75 %) ( Partial Albinism With Immunodeficiency,)
Moschcowitz Syndrome (75 %) ( Thrombotic Thrombocytopenic Purpura,)
Growth Hormone Deficiency (75 %)
Ocular Albinism (75 %)
Schilders Disease (75 %) ( Adrenoleukodystrophy,)
Oculocerebrorenal Dystrophy (75 %) ( Lowe Syndrome,)
Hereditary Periodic Fever Syndromes (75 %)
Partial Albinism With Immunodeficiency (75 %) ( Griscelli Syndrome Type2,)
Waardenburg Syndrome (75 %)
Body Dysmorphic Disorder (75 %) ( Dysmorphic Syndrome, Dysmorphophobia,)

Differentials from Google.

From Cache (Web service failed):

Ectodermal Dysplasia
Hidrotic Ectodermal Dysplasia
Hypohidrotic Ectodermal Dysplasia
Tooth And Nail Syndrome

Witkop Syndrome

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