Differentials: Adams oliver Syndrome

Differential diagnosis for Adams oliver 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 Adams oliver Syndrome.

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Date Added: 2017-09-23:

Papa Syndrome (100 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Marinesco sj gren Syndrome (100 %)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (100 %) ( Papa Syndrome,)
Tuberous Sclerosis (100 %) ( Bourneville Disease, Epiloia,)
Hypoparathyroidism (100 %)
Hyper-ige Syndrome (100 %) ( Buckley Syndrome, Job Syndrome,)
Cutis Laxa (86 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Apert Syndrome (86 %) ( Acrocephalosyndactyly,)
Acrocephalosyndactyly (86 %) ( Apert Syndrome,)
Lobstein Syndrome (86 %) ( Osteogenesis Imperfecta,)
Louis bar Syndrome (86 %) ( Ataxia Telangiectasia,)
Clubbing (86 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Johanson blizzard Syndrome (86 %)
Osteogenesis Imperfecta (86 %) ( Lobstein Syndrome,)
Chondrodysplasia Punctata (86 %)
Ataxia Telangiectasia (86 %) ( Louis bar Syndrome,)
Amniotic Band Syndrome (86 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Krabbe Disease (86 %)
Hurler Syndrome (86 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Familial Dysautonomia (86 %) ( Riley day Syndrome,)
Gunthers Disease (86 %) ( Congenital Erythropoietic Porphyria,)
Protoporphyria (86 %)
Ectodermal Dysplasia (86 %)
Infantile Myofibromatosis (86 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Digeorge Syndrome (86 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Riley day Syndrome (86 %) ( Familial Dysautonomia,)
Cartilage hair Hypoplasia (86 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Costello Syndrome (86 %)
Dyskeratosis Congenita (86 %) ( Zinsser cole engman Syndrome,)
Mucopolysaccharidosis Type Vii (86 %) ( Sly Syndrome,)
Adrenal Hyperplasia (86 %)
Hypophosphatasia (86 %)
Congenital Erythropoietic Porphyria (86 %) ( Gunthers Disease,)
Zinsser cole engman Syndrome (86 %) ( Dyskeratosis Congenita,)
Nevoid Basal Cell Carcinoma Syndrome (86 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Hypohidrotic Ectodermal Dysplasia (86 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Von Recklinghausens Disease (86 %) ( Neurofibromatosis Type1,)
Ehlers danlos Syndrome (86 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Aplasia Cutis Congenita (86 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Mucopolysaccharidosis Type Vi (86 %) ( Maroteaux lamy Syndrome,)
Spoon Nails (86 %) ( Koilonychia,)
Mckusick Type Metaphyseal Chondrodysplasia (86 %) ( Cartilage hair Hypoplasia,)
Koilonychia (86 %) ( Spoon Nails,)
Phenylketonuria (86 %)
Neurofibromatosis Type1 (86 %) ( Von Recklinghausens Disease,)
Erythropoietic Protoporphyria (86 %)
Peutz jeghers Syndrome (86 %)
Sly Syndrome (86 %) ( Mucopolysaccharidosis Type Vii,)
Maroteaux lamy Syndrome (86 %) ( Mucopolysaccharidosis Type Vi,)
X-linked Lymphoproliferative Disease (71 %) ( Duncans Disease,)
Cerebrotendinous Xanthomatosis (71 %)
HypervitaminosisA (71 %)
Glandular Fever (71 %) ( Infectious Mononucleosis,)
Duncans Disease (71 %) ( X-linked Lymphoproliferative Disease,)
Rubinstein taybi Syndrome (71 %)
Acquired Hypogammaglobulinemia (71 %) ( Common Variable Immunodeficiency,)
Centrofacial Lentiginosis (71 %)
Common Variable Immunodeficiency (71 %) ( Acquired Hypogammaglobulinemia,)
Immunodeficiency With Hyper-igm (71 %)
Carney Complex (71 %) ( Lamb Syndrome, Name Syndrome,)
Whim Syndrome (71 %) ( Warts hypogammaglobulinemia infections myelokathexis Syndrome,)
Segmental Neurofibromatosis (71 %)
Infectious Mononucleosis (71 %) ( Glandular Fever,)
Scurvy (71 %) ( VitaminC Deficiency,)
Fanconi Syndrome (71 %) ( Familial Pancytopenia, Familial Panmyelophthisis,)
Lymphangioma (71 %) ( Lymphangiectasis,)
Lymphangiectasis (71 %) ( Lymphangioma,)
Hyperphenylalaninemia (71 %)
Marfan Syndrome (71 %)
Pfeiffer Syndrome (71 %)
Progressive Osseous Heteroplasia (71 %)
Crouzon Syndrome (71 %)
Cardio-facio-cutaneous Syndrome (71 %) ( Cardiofaciocutaneous Syndrome,)
Cardiofaciocutaneous Syndrome (71 %) ( Cardio-facio-cutaneous Syndrome,)
Prader willi Syndrome (71 %)
Progeria (71 %) ( Hutchinson gilford Progeria Syndrome, Hutchinson gilford Syndrome, Progeria Syndrome,)
MucolipidosisI (71 %) ( Sialidosis,)
Partial Albinism With Immunodeficiency (71 %) ( Griscelli Syndrome Type2,)
Plaque-type Porokeratosis (71 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Sialidosis (71 %) ( MucolipidosisI,)
X-linked Hyper-igm Syndrome (71 %)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (71 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Majeed Syndrome (71 %)
Recessive Dystrophic Epidermolysis Bullosa (71 %) ( Hallopeau siemens Variant Of Epidermolysis Bullosa, Hallopeau siemens Disease,)
Warts hypogammaglobulinemia infections myelokathexis Syndrome (71 %) ( Whim Syndrome,)
HistiocytosisX (71 %) ( Langerhans Cell Histiocytosis,)
Griscelli Syndrome Type2 (71 %) ( Partial Albinism With Immunodeficiency,)
Pachydermoperiostosis (71 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Langerhans Cell Histiocytosis (71 %) ( HistiocytosisX,)
Tumor Lysis Syndrome (71 %)
VitaminC Deficiency (71 %) ( Scurvy,)
Mucolipidosis Type Ii (71 %) ( I-cell Disease,)
Alkaptonuria (71 %)
Moschcowitz Syndrome (71 %) ( Thrombotic Thrombocytopenic Purpura,)
Juvenile Systemic Hyalinosis (71 %) ( Infantile Systemic Hyalinosis,)
Fibrinolysis Syndrome (71 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Wiskott aldrich Syndrome (71 %)
Growth Hormone Deficiency (71 %)
Tumoral Calcinosis (71 %)
Ehlers-danlos Syndrome (71 %)
Gaucher Disease (71 %)
Berardinelli seip Syndrome (71 %) ( Congenital Generalized Lipodystrophy,)
Parry romberg Syndrome (71 %) ( Progressive Hemifacial Atrophy,)
Progressive Hemifacial Atrophy (71 %) ( Parry romberg Syndrome,)
Congenital Generalized Lipodystrophy (71 %) ( Berardinelli seip Syndrome,)
Cyanocobalamin Deficiency (71 %) ( VitaminB12 Deficiency,)
VitaminK Deficiency (71 %)
Lowry maclean Syndrome (71 %)
Thrombotic Thrombocytopenic Purpura (71 %) ( Moschcowitz Syndrome,)
VitaminB12 Deficiency (71 %) ( Cyanocobalamin Deficiency,)
Idiopathic Thrombocytopenic Purpura (71 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
Farber Disease (71 %) ( Fibrocytic Dysmucopolysaccharidosis, Lipogranulomatosis,)
Ataxia-telangiectasia (71 %)
Nail patella Syndrome (71 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Infantile Systemic Hyalinosis (71 %) ( Juvenile Systemic Hyalinosis,)
I-cell Disease (71 %) ( Mucolipidosis Type Ii,)
Turner Syndrome (71 %)
Chediak-higashi Syndrome (71 %)
Beare stevenson Cutis Gyrata Syndrome (71 %)
Goltz Syndrome (71 %) ( Focal Dermal Hypoplasia,)
Ch diak higashi Syndrome (71 %)
Torus Palatinus (71 %)
Severe Combined Immunodeficiency (71 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Focal Dermal Hypoplasia (71 %) ( Goltz Syndrome,)

Differentials from Google.

From Cache (Web service failed):
Aplasia Cutis Congenita
Mole

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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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