Differentials: Lig4 Syndrome

Differential diagnosis for Lig4 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 Lig4 Syndrome.

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Date Added: 2017-06-27:

Partial Albinism With Immunodeficiency (100 %) ( Griscelli Syndrome Type2,)
Digeorge Syndrome (100 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Common Variable Immunodeficiency (100 %) ( Acquired Hypogammaglobulinemia,)
Louis bar Syndrome (100 %) ( Ataxia Telangiectasia,)
Ataxia Telangiectasia (100 %) ( Louis bar Syndrome,)
Griscelli Syndrome Type2 (100 %) ( Partial Albinism With Immunodeficiency,)
Acquired Hypogammaglobulinemia (100 %) ( Common Variable Immunodeficiency,)
X-linked Hyper-igm Syndrome (100 %)
Severe Combined Immunodeficiency (100 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Ch diak higashi Syndrome (90 %)
Dyskeratosis Congenita (90 %) ( Zinsser cole engman Syndrome,)
Hyper-ige Syndrome (90 %) ( Buckley Syndrome, Job Syndrome,)
Diaper Candidiasis (90 %)
Ataxia-telangiectasia (90 %)
Chediak-higashi Syndrome (90 %)
Zinsser cole engman Syndrome (90 %) ( Dyskeratosis Congenita,)
Wiskott aldrich Syndrome (90 %)
Idiopathic Thrombocytopenic Purpura (80 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
X-linked Lymphoproliferative Disease (80 %) ( Duncans Disease,)
Whim Syndrome (80 %) ( Warts hypogammaglobulinemia infections myelokathexis Syndrome,)
Gaucher Disease (80 %)
Warts hypogammaglobulinemia infections myelokathexis Syndrome (80 %) ( Whim Syndrome,)
Duncans Disease (80 %) ( X-linked Lymphoproliferative Disease,)
Hypohidrotic Ectodermal Dysplasia (80 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Angioimmunoblastic Lymphadenopathy With Dysproteinemia (80 %) ( AngioimmunoblasticT-cell Lymphoma,)
HistiocytosisX (80 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (80 %) ( HistiocytosisX,)
Mckusick Type Metaphyseal Chondrodysplasia (80 %) ( Cartilage hair Hypoplasia,)
AngioimmunoblasticT-cell Lymphoma (80 %) ( Angioimmunoblastic Lymphadenopathy With Dysproteinemia,)
Cartilage hair Hypoplasia (80 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Majeed Syndrome (80 %)
Immunodeficiency With Hyper-igm (80 %)
Griscelli Syndrome (70 %)
Thrombotic Thrombocytopenic Purpura (70 %) ( Moschcowitz Syndrome,)
Acute Necrotizing Ulcerative Gingivitis (70 %) ( Acute Membranous Gingivitis, Acute Necrotizing Ulcerative Gingivostomatitis, Fusospirillary Gingivitis, Fusospirillosis, Fusospirochetal Gingivitis, Necrotizing Gingivitis, Phagedenic Gingivitis, Trench Mouth, Ulcerative Gingivitis, Vincent Gingivitis, Vincent Infection, Vincent Stomatitis, Vincents Disease,)
Hairy-cell Leukemia (70 %)
Bronze Diabetes (70 %) ( Hemochromatosis,)
Hemochromatosis (70 %) ( Bronze Diabetes,)
Krabbe Disease (70 %)
Piebaldism (70 %)
Roseola Infantum (70 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Polycythemia Vera (70 %) ( Erythremia,)
Gunthers Disease (70 %) ( Congenital Erythropoietic Porphyria,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (70 %) ( Papa Syndrome,)
Papa Syndrome (70 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Omenn Syndrome (70 %)
Congenital Erythropoietic Porphyria (70 %) ( Gunthers Disease,)
Sialidosis (70 %) ( MucolipidosisI,)
MucolipidosisI (70 %) ( Sialidosis,)
Juvenile Xanthogranuloma (70 %)
Folic Acid Deficiency (70 %)
Fanconi Syndrome (70 %) ( Familial Pancytopenia, Familial Panmyelophthisis,)
Papillon lef vre Syndrome (70 %) ( Palmoplantar Keratoderma With Periodontitis,)
Erythremia (70 %) ( Polycythemia Vera,)
Waldenstr m Macroglobulinemia (70 %)
Paroxysmal Nocturnal Hemoglobinuria (70 %)
Fibrinolysis Syndrome (70 %) ( Defibrinating Syndrome, Hypofibrinogenemia,)
Hurler Syndrome (70 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Farber Disease (70 %) ( Fibrocytic Dysmucopolysaccharidosis, Lipogranulomatosis,)
Erythropoietic Protoporphyria (70 %)
I-cell Disease (70 %) ( Mucolipidosis Type Ii,)
Tuberous Sclerosis (70 %) ( Bourneville Disease, Epiloia,)
Glandular Fever (70 %) ( Infectious Mononucleosis,)
Chondrodysplasia Punctata (70 %)
X-linked Agammaglobulinemia (70 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Moschcowitz Syndrome (70 %) ( Thrombotic Thrombocytopenic Purpura,)
Infectious Mononucleosis (70 %) ( Glandular Fever,)
Cutis Laxa (70 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Mucolipidosis Type Ii (70 %) ( I-cell Disease,)

Differentials from Google.

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Lig4 Syndrome

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