Genetics Articles

Article Name

21 Hydroxylase Deficiency
Abciximab
Abetalipoproteinemia
Acanthocytosis
Acoustic Neuroma (Vestibular Schwannoma)
Acquired Angioedema
Acquired Digital Fibrokeratoma
Acrodermatitis Enteropathica
Acrokeratoelastoidosis
Acrokeratosis Verruciformis of Hopf
Actinic Prurigo
Actinomycosis
Acute Ankle Sprain
Acute Intermittent Porphyria
Acute Myocardial Infarction
Acute Retinal Necrosis
Adrenal Hypoplasia
Aflatoxin Toxicity
Agammaglobulinemia
Aggression In Hypothalamic Hamartoma
Alagille Syndrome
Albinism
Alcoholic Neuropathy
Allopurinol
Alpha 1 Antitrypsin Deficiency
Alpha 1 Antitrypsin Mutation
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Alpha Thalassemia (Hemoglobin H Disease)
Alport Syndrome
Alzheimer Disease
Ambiguous Genitalia And Disorders of Sexual Differentiation
Amiloride
Amniotic Fluid Index (AFI)
Amyloid Beta Peptide
Amyotrophic Lateral Sclerosis
Anatomy, Abdomen and Pelvis, Seminal Vesicle
Anatomy, Abdomen and Pelvis, Sigmoid Colon
Anatomy, Bony Pelvis and Lower Limb, Foot
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Anatomy, Head and Neck, Nasal Cavity
Anatomy, Head and Neck, Occipital Bone, Artery, Vein, and Nerve
Anatomy, Head and Neck, Retropharyngeal Space
Anatomy, Head and Neck, Tooth Eruption
Anatomy, Thorax, Heart Anomalous Left Coronary Artery
Anatomy, Thorax, Tracheobronchial Tree
Androgen Insensitivity Syndrome
Angiodysplasia
Angioid Streaks (Knapp Streaks)
Angiokeratoma Circumscriptum
Anhidrosis
Aniridia
Antiemetic Serotonin-5-HT3 Receptor Blockers
Aortic Insufficiency
Aortic Regurgitation
Apert Syndrome
Aplasia Cutis Congenita
Aplastic Anemia
Apoptosis
Arginase Deficiency (Argininemia)
Arnold Chiari Malformation
Arrhythmogenic Right Ventricular Cardiomyopathy
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atopy
Atrial Septal Defect (ASD)
Atrioventricular Canal Defects
Autoimmune Myopathies (Dermatomyositis And Polymyositis)
Axenfeld Anomaly
Bartter Syndrome
Basal Cell Carcinoma
BAX Gene
Becker Muscular Dystrophy
Beevor Sign
Best Disease
Biochemistry, Antioxidants
Biochemistry, Apolipoprotein B
Biochemistry, Ceruloplasmin
Biochemistry, Chylomicron
Biochemistry, Citric Acid Cycle
Biochemistry, DNA Replication
Biochemistry, DNA Structure
Biochemistry, Dopamine Receptors
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Glycogenolysis
Biochemistry, HLA Antigens
Biochemistry, Immunoglobulin M (IgM)
Biochemistry, Ketone Metabolism
Biochemistry, LDL Cholesterol
Biochemistry, Lipids
Biochemistry, Lipoprotein Lipase
Biochemistry, Melanin
Biochemistry, Merosin
Biochemistry, Polymerase Chain Reaction (PCR)
Biochemistry, Presenilin
Biochemistry, Protein Catabolism
Biochemistry, Protein Synthesis
Biochemistry, Pseudogenes
Biochemistry, Replication and Transcription
Biochemistry, Substance P
Biochemistry, Superoxides
Biochemistry, Ubiquitination
Biochemstry, Fatty Acid Oxidation
Biotin Deficiency
Birdshot Retinopathy
Birt Hogg Dube Syndrome
Blighted Ovum (Anembryonic Pregnancy)
Bloom Syndrome (Congenital Telangiectatic Erythema)
Blue Nevus
Blue Rubber Bleb Nevus Syndrome
Bone Marrow Failure
Bone Marrow Transplantation In Sickle Cell Disease
Brachial Plexitis (Parsonage Turner Syndrome, Brachial Neuropathy, Brachial Radiculitis)
BRCA 1 and 2
Breast Cancer
Breast Magnetic Resonance Imaging (MRI)
Breast Milk Jaundice
Brugada Syndrome
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
C1 Esterase Inhibitor Deficiency
Cafe Au Lait Macules
Calcifying Epithelioma of Malherbe (Pilomatrixoma)
Canavan Disease
Cancer Breast Screening
Cancer, Ampullary
Cancer, Anaplastic Large Cell Lymphoma (ALCL Ki 1+)
Cancer, Anorexia and Cachexia
Cancer, Basal Cell
Cancer, Benign Mesothelioma
Cancer, Burkitt Lymphoma
Cancer, Chronic Myelogenous Leukemia (CML, Chronic Granulocytic Leukemia)
Cancer, Colon
Cancer, Endometrial
Cancer, Gastric
Cancer, Glomus (Glomangioma)
Cancer, Leukemia Cutis
Cancer, Lung Small Cell (Oat Cell)
Cancer, Lymphoplasmacytic Lymphoma (Waldenstrom Macroglobulinemia)
Cancer, Microcystic Adnexal Carcinoma (Sclerosing Sweat Gland)
Cancer, Neuroblastoma
Cancer, Ocular Melanoma
Cancer, Papillary Fibroelastoma
Cancer, Renal Cell
Cancer, Retinoblastoma
Cancer, T Cell Prolymphocytic Leukemia
Cancer, Tumor-Suppressor Genes
Cardiac Fibroma
Cardiac Manifestations Of Coronavirus (COVID-19)
Carney Complex
Caroli Disease
Catheter Management Of Ventricular Septal Defect
Cavernous Venous Malformation
Cavum Septum Pellucidum
Celiac Disease
Cerebral Amyloid Angiopathy
Cerebral Autosomal Dominant Arteriopathy (CADASIL)
Charcot Bouchard Aneurysm
Chediak Higashi Syndrome
Chemotherapy Acral Erythema (Palmar-Plantar Erythrodysesthesia, Palmoplantar Erythrodysesthesia, Hand-Foot Syndrome)
Cherry Red Spot
Chest Trauma
Chest Wall Deformities
Child Syndrome
Childhood Brain Tumors
Choanal Atresia
Chorea
Chromosome Instability Syndromes
Chronic Granulomatous Disease
Chronic Liver Disease
Chronic Testicular Pain (Orchialgia)
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Cleft Hand (Ectrodactyly, Split Hand)
Clinodactyly
Clostridium Difficile
Cockayne Syndrome
Colchicine
Colon Resection
Color Vision
Complement Deficiency
Congenital Adrenal Hyperplasia
Congenital Diaphragmatic Hernia
Congenital Hereditary Endothelial Dystrophy
Cooley Anemia
Copper Toxicity
Corneal Dystrophy
Cornelia de Lange Syndrome
Coronary Artery Anomalies
Coronary Cameral Fistula
Cough
Cowden Disease (Multiple Hamartoma Syndrome)
Craniopharyngioma
Craniosynostosis
Creutzfeldt Jakob Disease
Cri Du Chat Syndrome
Crohn Disease
Crouzon Syndrome
Cutaneous Leiomyomas
Cutis Laxa (Elastolysis)
Cyclic Neutropenia
Cylindroma
Cystic Fibrosis
Cystic Fibrosis And Liver Disease
Cystic Fibrosis Related Diabetes (CFRD)
Dandy Walker Malformation
Danon Disease
Delayed Puberty
Dermal Melanocytosis (Mongolian Spot), Congenital
Dermatosis Papulosa Nigra
Development Milestones
Dextrocardia
Diabetes, Maturity Onset in the Young (MODY)
Diamond Blackfan Anemia
DiGeorge Syndrome
Dornase Alfa
Dowling Degos Disease
Down Syndrome (Trisomy 21)
Drug Metabolism
Dubin Johnson Syndrome
Duchenne Muscular Dystrophy
Dyskeratosis Congenita
Dystonia
Dystonic Reactions
Dystrophinopathies
Ehlers Danlos Syndrome
Electrical Status Epilepticus In Sleep (ESES)
Embryology, Atrioventricular Septum
Embryology, Branchial Arches
Embryology, Central Nervous System, Malformations
Embryology, Ectoderm
Embryology, Epidermis
Embryology, Eye Malformations
Embryology, Gastrulation
Embryology, Kidney, Bladder, and Ureter
Embryology, Mullerian Ducts (Paramesonephric Ducts)
Embryology, Optic Cup
Embryology, Optic Fissure
Embryology, Pharyngeal Pouch
Embryology, Rectum and Anal Canal
Embryology, Sexual Development
Embryology, Uterus
Embryology, Wolffian Ducts
EMS, Chest Injury
Epidermodysplasia Verruciformis
Epidermolysis Bullosa Acquisita
Epidermolytic Hyperkeratosis (Bullous Ichthyosiform Erythroderma)
Eptifibatide
Erlotinib
Erythromelalgia
Essential Thrombocytosis (Essential Thrombocythemia, ET)
Extramammary Paget Disease
Fabry Disease
Factor XIII Deficiency
Familial Adenomatous Polyposis
Familial Hypercholesterolemia
Familial Hyperlipidemia Type 1
Familial Hyperlipidemia Type 2a
Familial Hypocalciuric Hypercalcemia (FHH)
Fanconi Syndrome
Fatal Familial Insomnia
Female Development
Fetal Alcohol Syndrome
Fibrous Dysplasia
Forensic Gait Analysis
Fragile X Syndrome
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
Fuchs Endothelial Dystrophy (FED)
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gaucher Disease
Generalized Pustular Psoriasis
Genetics, Autosomal Dominant
Genetics, Chromosome Abnormalities
Genetics, Chromosomes
Genetics, DNA Damage and Repair
Genetics, Epigenetic Mechanism
Genetics, Gonadal Dysgenesis
Genetics, Human Major Histocompatibility Complex (MHC)
Genetics, Nondisjunction
Genetics, Somatic Mutation
Genetics, Transposons
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Genetics, X-Linked Inheritance
Gilbert Syndrome
Gitelman Syndrome
Glanzmann Thrombasthenia
Gliomas
Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I (Von Gierke Disease)
Glycogen Storage Disease Type II (Pompe Disease)
Good Samaritan Laws
Goodpasture Syndrome (Anti-glomerular Basement Membrane Antibody Disease)
Gorlin Syndrome (Basal Cell Nevus)
Gout (Podagra)
Gynecomastia
Gyrate Atrophy Of The Choroid and Retina
Hallervorden Spatz Disease (Pantothenate Kinase-Associated Neurodegeneration, PKAN)
Health Screening
Hearing Loss
Hemarthrosis
Hemiplegic Migraine
Hemochromatosis
Hemolytic Diseases Of The Newborn
Hemolytic Uremic Syndrome (HUS)
Hemophilia
Hemophilia A
Hepatic (Hepatocellular) Adenoma
Hepatitis A
Hereditary Angioedema
Hereditary Spherocytosis
Herpes Zoster Ophthalmicus
Hirsutism
Histology, Astrocytes
Histology, Cell
Histology, Leydig Cells
Histology, Myelin
Histology, Parathyroid Gland
Histology, Plasma Cells
Histology, Retina
Histology, Spermatogenesis
Histology, T-Cell Lymphocyte
Histolology, Platelets
HLA B27 Syndromes
Hodgkin Lymphoma
Holt Oram Syndrome
Hurler Syndrome
Hydrocodone
Hyperacusis
Hypercalciuria
Hypercholesterolemia
Hyperhomocysteinemia
Hyperphosphatemia
Hyperpituitarism
Hypertrichosis
Hypertrophic Cardiomyopathy
Hypertrophic Obstructive Cardiomyopathy
Hypoaldosteronism
Hypomelanosis of Ito
Hypoparathyroidism
Hypospadias
Ichthyosis X-Linked
Idiopathic Guttate Hypomelanosis
IgA Nephropathy
Imatinib
Immunodeficiency
Immunotherapy
Impaired Bilirubin Conjugation
Imperforate Anus
Inborn Errors Of Metabolism
Infantile Cortical Hyperostosis (Caffey Disease)
Infantile Spasms
Informed Consent
Ingrown Toenails
Insulin Resistance
Insulinoma
Intellectual Disability
Interferon
Intestinal Trauma
Intravenous Immunoglobulin (IVIG)
Iron Overload
Jacobs (XYY) Syndrome
Jervell and Lange Nielsen Syndrome
Job Syndrome (Hyperimmunoglobulin E)
Juvenile Xanthogranuloma (Nevoxanthoendothelioma, JXG)
Kallmann Syndrome
Kearns Sayre Syndrome
Keratoendotheliitis Fugax Hereditaria
Keratosis Follicularis (Darier Disease)
Kidney Trauma
Klinefelter Syndrome
Lafora Disease
Landau Kleffner Syndrome
Latent Autoimmune Diabetes
Latex Allergy
Lattice Corneal Dystrophy
Laugier-Hunziker Syndrome
Learning Disability
Leber Optic Atrophy
Left Ventricular Non-compaction (LVNC) Cardiomyopathy
Lesch Nyhan Syndrome
Leukocyte Adhesion Deficiency
Li-Fraumeni Syndrome
Lipemia Retinalis
Lipodystrophies
Lipoid Pneumonia
Lipoma
Lisch Nodules
Liver Function Tests
Long QT Syndrome (LQTS)
Loose Anagen Syndrome
Lymphangioma
Lymphedema
Lymphoproliferative Disorders
Lynch Syndrome
Lytic Bone Lesions
Malabsorption Syndromes
Mallory Bodies
Mammary Duct Ectasia
Maple Syrup Urine Disease
Marfan Syndrome
May Hegglin Anomaly
McCune Albright Syndrome
Medulloblastoma
Megalocornea
Melas Syndrome
Mercaptopurine
Microcytic Hypochromic Anemia
Mitral Regurgitation
Mitral Valve Repair
Monilethrix
Moyamoya Disease
Muir-Torre Syndrome
Multiple Endocrine Neoplasia Type 1 (MEN I, Wermer Syndrome)
Multiple Endocrine Neoplasias, Type 2 (MEN II, Pheochromocytoma and Amyloid Producing Medullary Thyroid Carcinoma, Sipple Syndrome)
Multiple Sclerosis
Myelodysplastic Syndrome
Myeloperoxidase Deficiency
Myocardial Infarction
Myoclonic Epilepsy and Ragged Red Fibers (MERF)
Myotonic Dystrophy
Neural Tube Disorders
Neuroanatomy, Corticobulbar Tract
Neuroanatomy, Dentate Nucleus
Neuroanatomy, Lateral Corticospinal Tract
Neuroanatomy, Lower Motor Neuron Lesion
Neuroanatomy, Neural Tube Development and Stages
Neuroanatomy, Nucleus Caudate
Neuroanatomy, Touch Receptor
Neuroanatomy, Unmyelinated Nerve Fibers
Neurocutaneous Syndromes
Neurofibroma
Neurofibromatosis
Neurofibromatosis Type 1 (Von Recklinghausen)
Neurofibromatosis Type 2
Neuroma
Neuropathy
Nevus Comedonicus
Niemann-Pick Disease
Nonketotic Hyperglycinemia
Noonan Syndrome
Omphalocele
Open Angle Glaucoma
Optic Nerve Glioma
Ornithine Transcarbamylase Deficiency
Osler-Weber-Rendu Disease (Hereditary Hemorrhagic Telangiectasia, HHT)
Osteochondroma
Osteogenesis Imperfecta
Osteopetrosis
Paget Disease
Palmoplantar Psoriasis
Pancreatic Serous Cystadenoma
Pancrelipase Therapy
Patau Syndrome
Pectus Carinatum (Pigeon Chest)
Pediatric Functional Constipation
Pediatric Hearing Loss
Pemphigus Vegetans
Pendred Syndrome
Pericholangitis
Pernio (Chilblains)
Peutz-Jeghers Syndrome
Pfeiffer Syndrome
PHACE Syndrome
Phenylketonuria
Phenytoin
Photopic Vision
Physiology, Adenosine Triphosphate (ATP)
Physiology, Adrenal Gland
Physiology, Brain
Physiology, Cardiovascular Murmurs
Physiology, Cellular Receptor
Physiology, Chorionic Gonadotropin
Physiology, Factor V
Physiology, Follicle Stimulating Hormone
Physiology, Gluconeogenesis
Physiology, Gonadotropin Inhibitor
Physiology, Krebs Cycle
Physiology, Male Reproductive System
Physiology, Membrane
Physiology, Muscle
Physiology, Obesity Neurohormonal Appetite And Satiety Control
Physiology, Parathyroid
Physiology, Proteins
Physiology, Puberty
Physiology, Synuclein
Physiology, Thyroid
Physiology, Thyroid Function
Physiology, Vascular
Piebaldism
Piezogenic Pedal Papule
Pigmented Villonodular Synovitis
Pili Annulati
Poikiloderma Congenitale
Poland Syndrome
Polycystic Kidney Disease
Polycystic Kidney Disease Of Childhood
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Portal Vein Thrombosis
Prader-Willi Syndrome
Precocious Puberty
Preconception Counseling
Pregnancy Medications
Prenatal Genetic Screening
Prenatal Screening
Primary Amenorrhea
Primary Hyperparathyroidism
Progeria (Werner Syndrome)
Protein S and C
Prune Belly Syndrome
Pseudocholinesterase Deficiency
Pseudohypoparathyroidism
Pulmonary Hypertension
Pure Red Cell Aplasia
Raccoon Sign
Radial Dysplasia (Clubhand)
Radiology, Image Production and Evaluation
Reactive Perforating Collagenosis
Rectal Prolapse
Red Reflex
Reed Sternberg Cells
Renal Cyst
Renal Oncocytoma
Research Study
Restrictive (Infiltrative) Cardiomyopathy
Retinal Detachment
Retrognathia
Rett Syndrome
Right Aortic Arches
Rinne Test
Risk Factors For Coronary Artery Disease
Rotor Syndrome
Sertoli-Cell-Only Syndrome
Short Stature
Shwachman-Diamond Syndrome
Sickle Cell Anemia
Sickle Cell Trait
Single Ventricle
Sodium Nitroprusside
Spinocerebellar Ataxia
Splenic Sequestration Crisis
Sports Physicals
Steatorrhea
Stevens Johnson Syndrome (Toxic Epidermal Necrolysis)
Stewart-Treves Syndrome
Sturge-Weber Syndrome
Succinylcholine Chloride
Sudden Cardiac Death
Supravalvar Aortic Stenosis (SVAS)
Sweat Testing
Sydenham Chorea
Syndactyly
Syndromic Sensorineural Hearing Loss (SSHL)
Syringomyelia
Thalassemia
Thoracic Aorta Aneurysm
Thrombin
Thrombocytopenia
Thyroxine-Binding Globulin Deficiency
Tort
Tourette Syndrome And Other Tic Disorders
Tracheal Bronchus
Transposition Of The Great Arteries
Treadmill Stress Testing
Truncus Arteriosus
Tuberous Sclerosis
Tubular Adenoma
Turcot Syndrome
Turner Syndrome
Unconjugated Hyperbilirubinemia
Urea Cycle Disorders
Velocardiofacial Syndrome
Vismodegib
Vohwinkel Syndrome
Von Hippel Lindau Syndrome
Von Willebrand Disease
White Dot Syndromes
Williams Syndrome
Wilms Tumor (Nephroblastoma)
Wilson Disease
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum
Young Syndrome
Zinc Deficiency