Pediatric-Endocrinology Articles

Article Name

21 Hydroxylase Deficiency
5 Alpha Reductase Deficiency
Abetalipoproteinemia
Acanthocytosis
Achlorhydria
Achondroplasia
Acromegaly
Addison Disease
Adrenal Crisis
Adrenal Hypoplasia
Adrenal Insufficiency
Adrenocorticotropic Hormone Test (Cosyntropin Test)
Albright Hereditary Osteodystrophy
Ambiguous Genitalia And Disorders of Sexual Differentiation
Anabolic Steroids
Anatomy, Abdomen and Pelvis, Seminal Vesicle
Anatomy, Head and Neck, Parathyroid, Ectopic Glands
Anatomy, Head and Neck, Tonsils
Androgen Insensitivity Syndrome
Anorexia Nervosa
Anosmia
Antilipemic Agent Bile Acid Sequestrants
Arginase Deficiency (Argininemia)
Aspart Insulin
Ataxia Telangiectasia (Louis-Bar Syndrome)
Bilirubinuria
Biochemistry, Chylomicron
Biochemistry, Citric Acid Cycle
Biochemistry, Dihydrotestosterone
Biochemistry, Ghrelin
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Lipoprotein Lipase
Biochemistry, Protein Catabolism
Biochemistry, Pseudogenes
Biochemstry, Fatty Acid Oxidation
Biotin Deficiency
Bone Age
Bullosis Diabeticorum
C 17 Hydroxylase Deficiency
Cancer, Follicular Thyroid
Cancer, Medullary Thyroid
Carnitine Deficiency
Celiac Disease
Cerebral Edema
Cerebral Salt Wasting Syndrome
Chediak Higashi Syndrome
Child Abuse and Neglect
Chromosome Instability Syndromes
Cinacalcet
Congenital Adrenal Hyperplasia
Congenital Hypothyroidism
Constitutional Growth Delay
Cooling Techniques For Hyperthermia
Cushing Disease
Cushing Syndrome
Cystic Fibrosis And Liver Disease
Cystic Fibrosis Related Diabetes (CFRD)
Dawn Phenomenon
Delayed Puberty
Desmopressin
Diabetes Insipidus
Diabetes Mellitus Screening
Diabetes Mellitus Type 1
Diabetes Mellitus Type 1 In Children
Diabetic Embryopathy
Diabetic Foot Infections
Diffuse Toxic Goiter
DiGeorge Syndrome
Down Syndrome (Trisomy 21)
Ectopic Thyroid
Embryology, Pharyngeal Pouch
Embryology, Sexual Development
Euglycemic Diabetic Ketoacidosis
Factitious Hypoglycemia
Familial Adenomatous Polyposis
Familial Hypercholesterolemia
Familial Hyperlipidemia Type 1
Familial Hypocalciuric Hypercalcemia (FHH)
Familial Short Stature
Female Athlete Triad
Female Development
Fibrous Dysplasia
Fluorides and Fluorocarbons Toxicity
Fructosamine
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
Galactorrhea
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gardner Syndrome
Gender Dysphoria (Sexual Identity Disorders)
Genetics, X-Linked Inheritance
Gigantism And Acromegaly
Gitelman Syndrome
Glucagonoma Syndrome
Glucose Tolerance Test
Glycogen Storage Disease
Glycogen Storage Disease Type I (Von Gierke Disease)
Glycogen Storage Disease Type II (Pompe Disease)
Glycogenic Hepatopathy
Good Samaritan Laws
Gout (Podagra)
Graft Versus Host Disease
Graves Disease
Gyrate Atrophy Of The Choroid and Retina
Hartnup Disease
Hemolytic Diseases Of The Newborn
Hepatic Hemangioma
Hereditary Fructose Intolerance
High Anion Gap Metabolic Acidosis
Hirsutism
Histology, Leydig Cells
Histology, Parathyroid Gland
Human Insulin
Hurler Syndrome
Hyaluronidase
Hyperammonemia
Hyperphosphatemia
Hyperprolactinemia
Hyperthyroidism
Hyperthyroidism In Pregnancy
Hypoaldosteronism
Hypocalcemia
Hypokalemic Periodic Paralysis
Hypophosphatemia
Hypopituitarism (Panhypopituitarism)
I-123 Uptake
Inborn Errors Of Metabolism
Infantile Acne
Insulin Resistance
Insulinoma
Interrupted Aortic Arch
Jacobs (XYY) Syndrome
Kallmann Syndrome
Klinefelter Syndrome
Lafora Disease
Langerhans Cell Histiocytosis
Lesch Nyhan Syndrome
Leuprolide
Lipemia Retinalis
Lipodystrophies
Maple Syrup Urine Disease
Maturity Onset Diabetes in the Young (MODY)
McCune Albright Syndrome
Methimazole
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)
Munchausen Syndrome
Muscle Cramps
Neonatal Seizure
Neuroma
Newborn Subcutaneous Fat Necrosis
Nonketotic Hyperglycinemia
Obesity
Ornithine Transcarbamylase Deficiency
Orthostatic Hypotension
Osteoma Cutis
Osteopetrosis
Pancrelipase Therapy
Papillary Thyroid Carcinoma (PTC)
PCSK9 Inhibitors
Pediatric Craniopharyngioma
Pediatric Diabetic Ketoacidosis
Pediatric Type 2 Diabetes Mellitus
Pendred Syndrome
PHACE Syndrome
Phenytoin
Physiology, Adrenal Gland
Physiology, Bone Remodeling
Physiology, Gluconeogenesis
Physiology, Gonadotropin Inhibitor
Physiology, Gonadotropin-Releasing Hormone (GnRH)
Physiology, Leptin
Physiology, Opioid Receptor
Physiology, Osmoregulation and Excretion
Physiology, Parathyroid
Physiology, Puberty
Physiology, Sexual Maturity Rating
Physiology, Testosterone
Pituitary Adenoma
Polycystic Ovarian Disease (Stein-Leventhal Syndrome)
Polyglandular Autoimmune Syndrome Type I
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Post Transplant Lymphoproliferative Disorders
Prader-Willi Syndrome
Precocious Puberty
Primary Amenorrhea
Primary Hyperaldosteronism
Primary Hyperparathyroidism
Propylthiouracil (PTU)
Pseudohypoparathyroidism
Renal Tubular Acidosis
Retrognathia
Riesman Sign
Short Stature
Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
Syndromic Sensorineural Hearing Loss (SSHL)
Tanner Stages
Therapeutic Exercise
Thyroglossal Duct Cyst
Thyroid Nodule
Thyroiditis
Thyroxine-Binding Globulin Deficiency
Transposition Of The Great Arteries
Turner Syndrome
Urea Cycle Disorders
ViPoma
Vitamin B1 Thiamine Deficiency (Beriberi)
Vitamin D
Vitiligo
Waterhouse-Friderichsen Syndrome