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: 2018-02-06:

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

Differentials from Google.

Date Added: 2018-03-31

Allergic
Digeorge Anomaly

Hypoparathyroidism
Langerhans Cell Histiocytosis
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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