Differentials: Digeorge Anomaly

Differential diagnosis for Digeorge Anomaly

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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 Digeorge Anomaly.

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Date Added: 2017-08-07:

Digeorge Syndrome (100 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Tuberous Sclerosis (53 %) ( Bourneville Disease, Epiloia,)
Amniotic Band Syndrome (53 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Aplasia Cutis Congenita (47 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
HistiocytosisX (47 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (47 %) ( HistiocytosisX,)
Granulocytic Sarcoma (45 %) ( Chloroma, Myeloid Sarcoma,)
Ataxia Telangiectasia (42 %) ( Louis bar Syndrome,)
Louis bar Syndrome (42 %) ( Ataxia Telangiectasia,)
Juvenile Xanthogranuloma (42 %)
Wiskott aldrich Syndrome (42 %)
Severe Combined Immunodeficiency (42 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Hypohidrotic Ectodermal Dysplasia (42 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Cutis Laxa (42 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Cardio-facio-cutaneous Syndrome (42 %) ( Cardiofaciocutaneous Syndrome,)
Cardiofaciocutaneous Syndrome (42 %) ( Cardio-facio-cutaneous Syndrome,)
Bronze Diabetes (39 %) ( Hemochromatosis,)
Telangiectasia (39 %)
Common Variable Immunodeficiency (39 %) ( Acquired Hypogammaglobulinemia,)
Familial Dysautonomia (39 %) ( Riley day Syndrome,)
Clubbing (39 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Hemochromatosis (39 %) ( Bronze Diabetes,)
Costello Syndrome (39 %)
Acquired Hypogammaglobulinemia (39 %) ( Common Variable Immunodeficiency,)
Riley day Syndrome (39 %) ( Familial Dysautonomia,)
Hyper-ige Syndrome (39 %) ( Buckley Syndrome, Job Syndrome,)
Mucolipidosis Type Ii (37 %) ( I-cell Disease,)
Griscelli Syndrome Type2 (37 %) ( Partial Albinism With Immunodeficiency,)
Miliary Tuberculosis (37 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Partial Albinism With Immunodeficiency (37 %) ( Griscelli Syndrome Type2,)
Hay wells Syndrome (37 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Hurler Syndrome (37 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Dermatofibroma (37 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Tnf Receptor Associated Periodic Syndrome (37 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Majeed Syndrome (37 %)
Dyskeratosis Congenita (37 %) ( Zinsser cole engman Syndrome,)
I-cell Disease (37 %) ( Mucolipidosis Type Ii,)
Infantile Myofibromatosis (37 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Roseola Infantum (37 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Recurrent Aphthous Stomatitis (37 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Johanson blizzard Syndrome (37 %)
Chondrodysplasia Punctata (37 %)
Nasal Glioma (37 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Rhizomelic Chondrodysplasia Punctata (37 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Diffuse LargeB-cell Lymphoma (37 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Kabuki Syndrome (37 %) ( Kabuki Makeup Syndrome, Niikawa kuroki Syndrome,)
Zinsser cole engman Syndrome (37 %) ( Dyskeratosis Congenita,)
Angiocentric Lymphoma (37 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Primary Cutaneous LargeB-cell Lymphoma (37 %) ( Diffuse LargeB-cell Lymphoma,)
Callus (37 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Mucopolysaccharidosis Type Vi (34 %) ( Maroteaux lamy Syndrome,)
Maroteaux lamy Syndrome (34 %) ( Mucopolysaccharidosis Type Vi,)
Intravascular LargeB-cell Lymphoma (34 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Carney Complex (34 %) ( Lamb Syndrome, Name Syndrome,)
Gingival Hypertrophy (34 %)
Cyanocobalamin Deficiency (34 %) ( VitaminB12 Deficiency,)
Cyclic Neutropenia (34 %)
VitaminB12 Deficiency (34 %) ( Cyanocobalamin Deficiency,)
Juvenile Myelomonocytic Leukemia (34 %)
Lymphangioma (34 %) ( Lymphangiectasis,)
Body Dysmorphic Disorder (34 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Papa Syndrome (34 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Liposarcoma (34 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Acrochordon (34 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (34 %) ( Papa Syndrome,)
Lymphangiectasis (34 %) ( Lymphangioma,)
Selenium Deficiency (34 %)
4p- Syndrome (34 %) ( Wolf hirschhorn Syndrome,)
Chronic Granulomatous Disease (34 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Wolf hirschhorn Syndrome (34 %) ( 4p- Syndrome,)
Multiple Lentigines Syndrome (34 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (34 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Proteus Syndrome (34 %)
Rubinstein taybi Syndrome (34 %)
Neurofibromatosis Type1 (34 %) ( Von Recklinghausens Disease,)
Malignant Fibrous Histiocytoma (34 %)
Von Recklinghausens Disease (34 %) ( Neurofibromatosis Type1,)
Schwannoma (34 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Marfan Syndrome (34 %)
Thrombotic Thrombocytopenic Purpura (34 %) ( Moschcowitz Syndrome,)
Schinzel giedion Syndrome (34 %)
Mckusick Type Metaphyseal Chondrodysplasia (34 %) ( Cartilage hair Hypoplasia,)
Cartilage hair Hypoplasia (34 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Ectodermal Dysplasia (34 %)
Moschcowitz Syndrome (34 %) ( Thrombotic Thrombocytopenic Purpura,)

Differentials from Google.

Date Added: 2017-08-07

Digeorge Anomaly
Digeorge Syndrome

Thymic Hypoplasia
Wiskott-aldrich Syndrome

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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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