Differentials: severe combined immunodeficiency

Differential diagnosis for severe combined immunodeficiency

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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 severe combined immunodeficiency.

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Date Added: 2017-09-21:

Cutis Laxa (58 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
X-linked Hyper-igm Syndrome (55 %)
HistiocytosisX (55 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (55 %) ( HistiocytosisX,)
Acquired Hypogammaglobulinemia (55 %) ( Common Variable Immunodeficiency,)
Common Variable Immunodeficiency (55 %) ( Acquired Hypogammaglobulinemia,)
Wiskott aldrich Syndrome (55 %)
Digeorge Syndrome (52 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Dyskeratosis Congenita (48 %) ( Zinsser cole engman Syndrome,)
Hypohidrotic Ectodermal Dysplasia (48 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Zinsser cole engman Syndrome (48 %) ( Dyskeratosis Congenita,)
Ataxia Telangiectasia (48 %) ( Louis bar Syndrome,)
Infectious Mononucleosis (48 %) ( Glandular Fever,)
Acrochordon (48 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Glandular Fever (48 %) ( Infectious Mononucleosis,)
Louis bar Syndrome (48 %) ( Ataxia Telangiectasia,)
Juvenile Xanthogranuloma (48 %)
Majeed Syndrome (45 %)
Cutaneous Lymphoid Hyperplasia (45 %) ( 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,)
Chronic Granulomatous Disease (45 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Partial Albinism With Immunodeficiency (45 %) ( Griscelli Syndrome Type2,)
Griscelli Syndrome Type2 (45 %) ( Partial Albinism With Immunodeficiency,)
X-linked Agammaglobulinemia (45 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Hyper-ige Syndrome (45 %) ( Buckley Syndrome, Job Syndrome,)
Idiopathic Thrombocytopenic Purpura (45 %) ( Autoimmune Thrombocytopenic Purpura, Werlhofs Disease,)
Angiocentric Lymphoma (45 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Tuberous Sclerosis (45 %) ( Bourneville Disease, Epiloia,)
Tnf Receptor Associated Periodic Syndrome (42 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Ataxia-telangiectasia (42 %)
Schwannoma (42 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Adrenal Hyperplasia (42 %)

Differentials from Google.

Date Added: 2017-11-08

Digeorge Syndrome

Erythroderma
Severe Combined Immunodeficiency

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