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: 2017-02-04:

Digeorge Syndrome (100 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Tuberous Sclerosis (54 %) ( Bourneville Disease, Epiloia,)
Amniotic Band Syndrome (54 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Aplasia Cutis Congenita (49 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Langerhans Cell Histiocytosis (49 %) ( HistiocytosisX,)
HistiocytosisX (49 %) ( Langerhans Cell Histiocytosis,)
Granulocytic Sarcoma (46 %) ( Chloroma, Myeloid Sarcoma,)
Louis bar Syndrome (43 %) ( Ataxia Telangiectasia,)
Ataxia Telangiectasia (43 %) ( Louis bar Syndrome,)
Cardio-facio-cutaneous Syndrome (43 %) ( Cardiofaciocutaneous Syndrome,)
Severe Combined Immunodeficiency (43 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Cutis Laxa (43 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Cardiofaciocutaneous Syndrome (43 %) ( Cardio-facio-cutaneous Syndrome,)
Juvenile Xanthogranuloma (43 %)
Hypohidrotic Ectodermal Dysplasia (43 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Wiskott aldrich Syndrome (43 %)
Familial Dysautonomia (41 %) ( Riley day Syndrome,)
Common Variable Immunodeficiency (41 %) ( Acquired Hypogammaglobulinemia,)
Riley day Syndrome (41 %) ( Familial Dysautonomia,)
Bronze Diabetes (41 %) ( Hemochromatosis,)
Costello Syndrome (41 %)
Clubbing (41 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Hyper-ige Syndrome (41 %) ( Buckley Syndrome, Job Syndrome,)
Acquired Hypogammaglobulinemia (41 %) ( Common Variable Immunodeficiency,)
Telangiectasia (41 %)
Hemochromatosis (41 %) ( Bronze Diabetes,)
Tnf Receptor Associated Periodic Syndrome (38 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Nasal Glioma (38 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Mucolipidosis Type Ii (38 %) ( I-cell Disease,)
Infantile Myofibromatosis (38 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Angiocentric Lymphoma (38 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Dermatofibroma (38 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Johanson blizzard Syndrome (38 %)
Roseola Infantum (38 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Rhizomelic Chondrodysplasia Punctata (38 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Hay wells Syndrome (38 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
I-cell Disease (38 %) ( Mucolipidosis Type Ii,)
Partial Albinism With Immunodeficiency (38 %) ( Griscelli Syndrome Type2,)
Recurrent Aphthous Stomatitis (38 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Zinsser cole engman Syndrome (38 %) ( Dyskeratosis Congenita,)
Miliary Tuberculosis (38 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Griscelli Syndrome Type2 (38 %) ( Partial Albinism With Immunodeficiency,)
Dyskeratosis Congenita (38 %) ( Zinsser cole engman Syndrome,)
Majeed Syndrome (38 %)
Hurler Syndrome (38 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Chondrodysplasia Punctata (38 %)
Diffuse LargeB-cell Lymphoma (38 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Primary Cutaneous LargeB-cell Lymphoma (38 %) ( Diffuse LargeB-cell Lymphoma,)
Callus (38 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Kabuki Syndrome (38 %) ( Kabuki Makeup Syndrome, Niikawa kuroki Syndrome,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (35 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Gingival Hypertrophy (35 %)
Cyclic Neutropenia (35 %)
Body Dysmorphic Disorder (35 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
VitaminB12 Deficiency (35 %) ( Cyanocobalamin Deficiency,)
Ectodermal Dysplasia (35 %)
Juvenile Myelomonocytic Leukemia (35 %)
Thrombotic Thrombocytopenic Purpura (35 %) ( Moschcowitz Syndrome,)
Mucopolysaccharidosis Type Vi (35 %) ( Maroteaux lamy Syndrome,)
Schinzel giedion Syndrome (35 %)
Malignant Fibrous Histiocytoma (35 %)
Intravascular LargeB-cell Lymphoma (35 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Moschcowitz Syndrome (35 %) ( Thrombotic Thrombocytopenic Purpura,)
Schwannoma (35 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Maroteaux lamy Syndrome (35 %) ( Mucopolysaccharidosis Type Vi,)
Papa Syndrome (35 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Marfan Syndrome (35 %)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (35 %) ( Papa Syndrome,)
Liposarcoma (35 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Wolf hirschhorn Syndrome (35 %) ( 4p- Syndrome,)
Acrochordon (35 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Carney Complex (35 %) ( Lamb Syndrome, Name Syndrome,)
Multiple Lentigines Syndrome (35 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Rubinstein taybi Syndrome (35 %)
Lymphangiectasis (35 %) ( Lymphangioma,)
Lymphangioma (35 %) ( Lymphangiectasis,)
4p- Syndrome (35 %) ( Wolf hirschhorn Syndrome,)
Cyanocobalamin Deficiency (35 %) ( VitaminB12 Deficiency,)
Selenium Deficiency (35 %)
Proteus Syndrome (35 %)
Neurofibromatosis Type1 (35 %) ( Von Recklinghausens Disease,)
Mckusick Type Metaphyseal Chondrodysplasia (35 %) ( Cartilage hair Hypoplasia,)
Chronic Granulomatous Disease (35 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Cartilage hair Hypoplasia (35 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Von Recklinghausens Disease (35 %) ( Neurofibromatosis Type1,)

Differentials from Google.

Date Added: 2017-02-05

Digeorge Anomaly
Digeorge Syndrome

Thymic Hypoplasia

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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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