Differentials: Familial Defective Apolipoprotein B-100

Differential diagnosis for Familial Defective Apolipoprotein B-100

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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 Familial Defective Apolipoprotein B-100.

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Date Added: 2017-06-07:

Ehlers danlos Syndrome (100 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Hereditary Hemorrhagic Telangiectasia (88 %) ( Oslers Disease, Osler weber rendu Disease,)
Wooly Hair (88 %) ( Woolly Hair,)
Multiple Endocrine Neoplasia Type2 (88 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Woolly Hair (88 %) ( Wooly Hair,)
Cutis Laxa (88 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Body Dysmorphic Disorder (88 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Palmoplantar Keratoderma (88 %)
Ehlers-danlos Syndrome (88 %)
Tuberous Sclerosis (88 %) ( Bourneville Disease, Epiloia,)
Neurofibromatosis Type1 (75 %) ( Von Recklinghausens Disease,)
Noonan Syndrome (75 %)
Treacher Collins franceschetti Syndrome (75 %) ( Treacher Collins Syndrome,)
Treacher Collins Syndrome (75 %) ( Treacher Collins franceschetti Syndrome,)
Multiple Lentigines Syndrome (75 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Neurofibromatosis Type1-like Syndrome (75 %) ( Legius Syndrome,)
Marfan Syndrome (75 %)
Liposarcoma (75 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Telangiectasia (75 %)
Costello Syndrome (75 %)
Legius Syndrome (75 %) ( Neurofibromatosis Type1-like Syndrome,)
Carney Complex (75 %) ( Lamb Syndrome, Name Syndrome,)
Rubinstein taybi Syndrome (75 %)
Refsum Disease (75 %)
Familial Mediterranean Fever (75 %)
Clubbing (75 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Familial Amyloid Polyneuropathy (75 %)
Posterior Fossa Malformations hemangiomas arterial Anomalies cardiac Defects eye Abnormalities sternal Cleft And Supraumbilical Raphe Syndrome (75 %) ( Phace Association, Phaces Syndrome,)
Supernumerary Nipple (75 %) ( Accessory Nipple, Pseudomamma,)
Digeorge Syndrome (75 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Fabry Disease (75 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Von Recklinghausens Disease (75 %) ( Neurofibromatosis Type1,)
Naxos Syndrome (75 %) ( Diffuse Non-epidermolytic Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Diffuse Palmoplantar Keratoderma With Woolly Hair And Arrythmogenic Right Ventricular Cardiomyopathy Of Naxos, Naxos Disease,)
Amniotic Band Syndrome (75 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Peutz jeghers Syndrome (63 %)
Dolichol Kinase Deficiency (63 %)
Cerebrotendinous Xanthomatosis (63 %)
Hunter Syndrome (63 %)
Cardiofaciocutaneous Syndrome (63 %) ( Cardio-facio-cutaneous Syndrome,)
Zoster (63 %) ( Herpes Zoster, Shingles,)
Acrocephalosyndactyly (63 %) ( Apert Syndrome,)
Smooth Tongue (63 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Adult Progeria (63 %) ( Werner Syndrome,)
Fissured Tongue (63 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Disease (63 %)
Freckles (63 %) ( Ephelides,)
Acroosteolysis (63 %)
Ephelides (63 %) ( Freckles,)
Hypoparathyroidism (63 %)
Basal Cell Carcinoma (63 %)
Angioedema (63 %)
Johanson blizzard Syndrome (63 %)
Goltz Syndrome (63 %) ( Focal Dermal Hypoplasia,)
Focal Dermal Hypoplasia (63 %) ( Goltz Syndrome,)
Deep Venous Thrombosis (63 %)
Cardio-facio-cutaneous Syndrome (63 %) ( Cardiofaciocutaneous Syndrome,)
Orofaciodigital Syndrome (63 %)
Rhizomelic Chondrodysplasia Punctata (63 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Neutral Lipid Storage Disease (63 %) ( Dorfman chanarin Syndrome,)
Chondrodysplasia Punctata (63 %)
Dorfman chanarin Syndrome (63 %) ( Neutral Lipid Storage Disease,)
Watson Syndrome (63 %)
Dermatofibroma (63 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Acute Intermittent Porphyria (63 %)
Carvajal Syndrome (63 %) ( Striate Palmoplantar Keratoderma With Woolly Hair And Cardiomyopathy, Striate Palmoplantar Keratoderma With Woolly Hair And Left Ventricular Dilated Cardiomyopathy,)
Familial Partial Lipodystrophy (63 %) ( K bberling dunnigan Syndrome,)
Acquired Generalized Lipodystrophy (63 %) ( Lawrence Syndrome, Lawrence seip Syndrome,)
K bberling dunnigan Syndrome (63 %) ( Familial Partial Lipodystrophy,)
Glomus Tumor (63 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Intrahepatic Cholestasis Of Pregnancy (63 %) ( Cholestasis Of Pregnancy, Jaundice Of Pregnancy, Obstetric Cholestasis, Prurigo Gravidarum,)
Growth Hormone Deficiency (63 %)
Moschcowitz Syndrome (63 %) ( Thrombotic Thrombocytopenic Purpura,)
Sitosterolemia (63 %) ( Phytosterolemia,)
Torus Palatinus (63 %)
Cyclic Neutropenia (63 %)
Mucopolysaccharidosis Type Vi (63 %) ( Maroteaux lamy Syndrome,)
Mucolipidosis Type Ii (63 %) ( I-cell Disease,)
I-cell Disease (63 %) ( Mucolipidosis Type Ii,)
X-linked Ichthyosis (63 %) ( Steroid Sulfatase Deficiency, X-linked Recessive Ichthyosis,)
Carnitine Deficiency (63 %)
Angiokeratoma (63 %)
Hurler Syndrome (63 %) ( Gargoylism, Mucopolysaccharidosis TypeI,)
Erythropoietic Protoporphyria (63 %)
Keratosis Pilaris Atrophicans Faciei (63 %) ( Folliculitis Rubra, Keratosis Pilaris Rubra Atrophicans Faciei, Lichen Pilare, Lichen Pilaire Ou Xerodermie Pilaire Symmetrique De La Face, Ulerythema Ophryogenes, Xerodermi Pilaire Symmetrique De La Face,)
Werner Syndrome (63 %) ( Adult Progeria,)
Oculodentodigital Dysplasia (63 %)
Riley day Syndrome (63 %) ( Familial Dysautonomia,)
Maroteaux lamy Syndrome (63 %) ( Mucopolysaccharidosis Type Vi,)
Familial Dysautonomia (63 %) ( Riley day Syndrome,)
Thrombotic Thrombocytopenic Purpura (63 %) ( Moschcowitz Syndrome,)
Chronic Granulomatous Disease (63 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Variegate Porphyria (63 %) ( Mixed Hepatic Porphyria, Mixed Porphyria, South African Genetic Porphyria, South African Porphyria,)
Phytosterolemia (63 %) ( Sitosterolemia,)
Apert Syndrome (63 %) ( Acrocephalosyndactyly,)
Hypohidrosis (63 %) ( Anhidrosis,)
Bronze Diabetes (63 %) ( Hemochromatosis,)
Congenital Generalized Lipodystrophy (63 %) ( Berardinelli seip Syndrome,)
Berardinelli seip Syndrome (63 %) ( Congenital Generalized Lipodystrophy,)
Anhidrosis (63 %) ( Hypohidrosis,)
Hyperparathyroidism (63 %)
Hemochromatosis (63 %) ( Bronze Diabetes,)

Differentials from Google.

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Iron Deficiency

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