Differentials: Angelman Syndrome

Differential diagnosis for Angelman 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 Angelman Syndrome.

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Date Added: 2017-12-08:

Wiskott aldrich Syndrome (100 %)
Tuberous Sclerosis (100 %) ( Bourneville Disease, Epiloia,)
Familial Dysautonomia (100 %) ( Riley day Syndrome,)
Riley day Syndrome (100 %) ( Familial Dysautonomia,)
Amniotic Band Syndrome (100 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Folic Acid Deficiency (89 %)
Farber Disease (89 %) ( Fibrocytic Dysmucopolysaccharidosis, Lipogranulomatosis,)
Cerebrotendinous Xanthomatosis (89 %)
Griscelli Syndrome Type2 (89 %) ( Partial Albinism With Immunodeficiency,)
Mucopolysaccharidosis Type Vi (89 %) ( Maroteaux lamy Syndrome,)
Partial Albinism With Immunodeficiency (89 %) ( Griscelli Syndrome Type2,)
Chondrodysplasia Punctata (89 %)
Growth Hormone Deficiency (89 %)
Nail patella Syndrome (89 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Gaucher Disease (89 %)
HistiocytosisX (89 %) ( Langerhans Cell Histiocytosis,)
Digeorge Syndrome (89 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Cutis Laxa (89 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Hemochromatosis (89 %) ( Bronze Diabetes,)
Bronze Diabetes (89 %) ( Hemochromatosis,)
Langerhans Cell Histiocytosis (89 %) ( HistiocytosisX,)
Maroteaux lamy Syndrome (89 %) ( Mucopolysaccharidosis Type Vi,)
Mucopolysaccharidosis Type Vii (78 %) ( Sly Syndrome,)
Conradi h nermann Syndrome (78 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Papillon lef vre Syndrome (78 %) ( Palmoplantar Keratoderma With Periodontitis,)
Roseola Infantum (78 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Ehlers danlos Syndrome (78 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Thrombotic Thrombocytopenic Purpura (78 %) ( Moschcowitz Syndrome,)
Sialidosis (78 %) ( MucolipidosisI,)
Cartilage hair Hypoplasia (78 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Sly Syndrome (78 %) ( Mucopolysaccharidosis Type Vii,)
Hurler Syndrome (78 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Infantile Myofibromatosis (78 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Cyanocobalamin Deficiency (78 %) ( VitaminB12 Deficiency,)
Ataxia Telangiectasia (78 %) ( Louis bar Syndrome,)
Encephalocele (78 %)
Louis bar Syndrome (78 %) ( Ataxia Telangiectasia,)
Mckusick Type Metaphyseal Chondrodysplasia (78 %) ( Cartilage hair Hypoplasia,)
Marinesco sj gren Syndrome (78 %)
Hyperphenylalaninemia (78 %)
Hypohidrotic Ectodermal Dysplasia (78 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Neurofibromatosis Type1 (78 %) ( Von Recklinghausens Disease,)
Moschcowitz Syndrome (78 %) ( Thrombotic Thrombocytopenic Purpura,)
Fibrinolysis Syndrome (78 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Ehlers-danlos Syndrome (78 %)
I-cell Disease (78 %) ( Mucolipidosis Type Ii,)
Mucolipidosis Type Ii (78 %) ( I-cell Disease,)
Klippel feil Syndrome (78 %)
Proteus Syndrome (78 %)
MucolipidosisI (78 %) ( Sialidosis,)
Progeria (78 %) ( Hutchinson gilford Progeria Syndrome, Hutchinson gilford Syndrome, Progeria Syndrome,)
Congenital Melanocytic Nevus (78 %)
Aplasia Cutis Congenita (78 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
X-linked Lymphoproliferative Disease (78 %) ( Duncans Disease,)
Duncans Disease (78 %) ( X-linked Lymphoproliferative Disease,)
Von Recklinghausens Disease (78 %) ( Neurofibromatosis Type1,)
Apert Syndrome (78 %) ( Acrocephalosyndactyly,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (78 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
VitaminB12 Deficiency (78 %) ( Cyanocobalamin Deficiency,)
Adrenal Hyperplasia (78 %)
Clubbing (78 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Callus (78 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Cardio-facio-cutaneous Syndrome (78 %) ( Cardiofaciocutaneous Syndrome,)
Cardiofaciocutaneous Syndrome (78 %) ( Cardio-facio-cutaneous Syndrome,)
Selenium Deficiency (78 %)
Prader willi Syndrome (78 %)
Krabbe Disease (78 %)
Johanson blizzard Syndrome (78 %)
Acrocephalosyndactyly (78 %) ( Apert Syndrome,)
Hyper-ige Syndrome (78 %) ( Buckley Syndrome, Job Syndrome,)
Hyperparathyroidism (78 %)
Soft-tissue Melanoma (78 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (67 %) ( Papa Syndrome,)
Body Dysmorphic Disorder (67 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Ectodermal Dysplasia (67 %)
Mucopolysaccharidosis TypeIH-s (67 %) ( Hurler scheie Syndrome,)
Arthrogryposis renal Dysfunction cholestasis Syndrome (67 %) ( Arc Syndrome,)
Waldenstr m Macroglobulinemia (67 %)
VitaminB6 Deficiency (67 %) ( Pyridoxine Deficiency,)
Pyridoxine Deficiency (67 %) ( VitaminB6 Deficiency,)
Dermatofibrosis Lenticularis Disseminata (67 %) ( Buschke ollendorff Syndrome,)
Ochronosis (67 %)
Hurler scheie Syndrome (67 %) ( Mucopolysaccharidosis TypeIH-s,)
Arc Syndrome (67 %) ( Arthrogryposis renal Dysfunction cholestasis Syndrome,)
Mucopolysaccharidosis TypeIS (67 %) ( Scheie Syndrome,)
Warts hypogammaglobulinemia infections myelokathexis Syndrome (67 %) ( Whim Syndrome,)
Schimmelpenning feuerstein mims Syndrome (67 %) ( Schimmelpenning Syndrome,)
Epidermal Nevus Syndrome (67 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Rosai dorfman Disease (67 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Tumoral Calcinosis (67 %)
Schimmelpenning Syndrome (67 %) ( Schimmelpenning feuerstein mims Syndrome,)
Ataxia-telangiectasia (67 %)
Costello Syndrome (67 %)
Papa Syndrome (67 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Juvenile Xanthogranuloma (67 %)
Idiopathic Thrombocytopenic Purpura (67 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
VitaminK Deficiency (67 %)
Triangular Alopecia (67 %) ( Temporal Alopecia, Temporal Triangular Alopecia,)
Coccidioidomycosis (67 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Infectious Mononucleosis (67 %) ( Glandular Fever,)
Glandular Fever (67 %) ( Infectious Mononucleosis,)
Scurvy (67 %) ( VitaminC Deficiency,)
X-linked Hyper-igm Syndrome (67 %)
Merkel Cell Carcinoma (67 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Hypophosphatasia (67 %)
Congenital Generalized Lipodystrophy (67 %) ( Berardinelli seip Syndrome,)
Berardinelli seip Syndrome (67 %) ( Congenital Generalized Lipodystrophy,)
VitaminC Deficiency (67 %) ( Scurvy,)
Alkaptonuria (67 %)
Carney Complex (67 %) ( Lamb Syndrome, Name Syndrome,)
Albrights Disease (67 %) ( Polyostotic Fibrous Dysplasia,)
Chediak-higashi Syndrome (67 %)
Disease (67 %)
Fibrodysplasia Ossificans Progressiva (67 %)
Ch diak higashi Syndrome (67 %)
Erythropoietic Protoporphyria (67 %)
Mccune albright Syndrome (67 %)
Majeed Syndrome (67 %)
Gunthers Disease (67 %) ( Congenital Erythropoietic Porphyria,)
Phenylketonuria (67 %)
Loeys dietz Syndrome (67 %)
Oculodentodigital Dysplasia (67 %)
Fanconi Syndrome (67 %) ( Familial Pancytopenia, Familial Panmyelophthisis,)
Juvenile Myelomonocytic Leukemia (67 %)
Hairy-cell Leukemia (67 %)
Acrochordon (67 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Liposarcoma (67 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Whim Syndrome (67 %) ( Warts hypogammaglobulinemia infections myelokathexis Syndrome,)
Buschke ollendorff Syndrome (67 %) ( Dermatofibrosis Lenticularis Disseminata,)
Anonychia (67 %)
Adrenal Adenoma (67 %)
Common Variable Immunodeficiency (67 %) ( Acquired Hypogammaglobulinemia,)
Acquired Hypogammaglobulinemia (67 %) ( Common Variable Immunodeficiency,)
Sinus Histiocytosis With Massive Lymphadenopathy (67 %) ( Rosai dorfman Disease,)
Congenital Erythropoietic Porphyria (67 %) ( Gunthers Disease,)
Osteogenesis Imperfecta (67 %) ( Lobstein Syndrome,)
Lobstein Syndrome (67 %) ( Osteogenesis Imperfecta,)
Peutz jeghers Syndrome (67 %)
Gingival Hypertrophy (67 %)
Hypoparathyroidism (67 %)
Fibrodysplasia Ossificans (67 %)
Scheie Syndrome (67 %) ( Mucopolysaccharidosis TypeIS,)
Crouzon Syndrome (67 %)
Schwannoma (67 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Chromoblastomycosis (67 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Polycythemia Vera (67 %) ( Erythremia,)
Recessive Dystrophic Epidermolysis Bullosa (67 %) ( Hallopeau siemens Variant Of Epidermolysis Bullosa, Hallopeau siemens Disease,)
4p- Syndrome (67 %) ( Wolf hirschhorn Syndrome,)
Systemic Mastocytosis (67 %)
Rubinstein taybi Syndrome (67 %)
Immunodeficiency With Hyper-igm (67 %)
Zinsser cole engman Syndrome (67 %) ( Dyskeratosis Congenita,)
Human Herpesvirus6 (67 %)
Pachydermoperiostosis (67 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Parry romberg Syndrome (67 %) ( Progressive Hemifacial Atrophy,)
Nevoid Basal Cell Carcinoma Syndrome (67 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Dyskeratosis Congenita (67 %) ( Zinsser cole engman Syndrome,)
Rhizomelic Chondrodysplasia Punctata (67 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Erythremia (67 %) ( Polycythemia Vera,)
Granulocytic Sarcoma (67 %) ( Chloroma, Myeloid Sarcoma,)
Wolf hirschhorn Syndrome (67 %) ( 4p- Syndrome,)
Lig4 Syndrome (67 %)
Goltz Syndrome (67 %) ( Focal Dermal Hypoplasia,)
Focal Dermal Hypoplasia (67 %) ( Goltz Syndrome,)
Polyostotic Fibrous Dysplasia (67 %) ( Albrights Disease,)
Iron Deficiency (67 %)
Meningocele (67 %)
Pfeiffer Syndrome (67 %)
Turner Syndrome (67 %)
Progressive Hemifacial Atrophy (67 %) ( Parry romberg Syndrome,)
Severe Combined Immunodeficiency (67 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)

Differentials from Google.

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Angelman Syndrome

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