Pediatric-Developmental Articles

Article Name

21 Hydroxylase Deficiency
5 Alpha Reductase Deficiency
Abetalipoproteinemia
Absence Seizure
Acanthocytosis
Achondroplasia
Acrodermatitis Enteropathica
Acute Otitis Media
Acute Scrotum Pain
Adrenal Hypoplasia
Aflatoxin Toxicity
Aggression In Hypothalamic Hamartoma
Agitation
Airway Suctioning
Alagille Syndrome
Albinism
Albright Hereditary Osteodystrophy
Allergic Rhinitis
Alpers-Huttenlocher Syndrome (AHS, Alper Disease)
Alpha Fetoprotein (AFP, Maternal Serum Alpha Fetoprotein, MSAFP)
Ambiguous Genitalia And Disorders of Sexual Differentiation
Amblyopia
Amiloride
Amniotic Band Syndrome
Amphetamine
Anatomy, Abdomen and Pelvis, Inguinal Lymph Node
Anatomy, Abdomen and Pelvis, Pelvic Outlet
Anatomy, Abdomen and Pelvis, Penis
Anatomy, Abdomen and Pelvis, Scrotum
Anatomy, Abdomen and Pelvis, Sigmoid Colon
Anatomy, Bony Pelvis and Lower Limb, Foot
Anatomy, Head and Neck, Eye Arteries
Anatomy, Head and Neck, Eye Iris Sphincter Muscle
Anatomy, Head and Neck, Frontalis Muscle
Anatomy, Head and Neck, Glabella
Anatomy, Head and Neck, Nasal Cavity
Anatomy, Head and Neck, Nose
Anatomy, Head and Neck, Palate
Anatomy, Head and Neck, Tongue
Anatomy, Head and Neck, Tooth Eruption
Anatomy, Patient Positioning
Anemia, Iron Deficiency
Angioid Streaks (Knapp Streaks)
Angiokeratoma Circumscriptum
Anhidrosis
Aniridia
Ankyloglossia
Annular Pancreas
Anosmia
Anovulatory Bleeding
Anthropometric Measurement
Antidepressants
Aortic Valvular Atresia
Apert Syndrome
Aplasia Cutis Congenita
Apnea In Children
Arginase Deficiency (Argininemia)
Arnold Chiari Malformation
Art Therapy
Asperger Syndrome
Ataxia Telangiectasia (Louis-Bar Syndrome)
Atrial Septal Defect (ASD)
Atrioventricular Canal Defects
Attention Deficit Hyperactivity Disorder (ADHD)
Autism Spectrum Disorder (Regressive Autism, Child Disintegrative Disorder)
Bartter Syndrome
Becker Muscular Dystrophy
Beckwith Wiedemann Syndrome
Beevor Sign
Behavior Modification
Benazepril
Benign Occipital Seizure
Bicuspid Aortic Valve
Biliary Atresia
Biochemistry, Ammonia
Biochemistry, Ceruloplasmin
Biochemistry, Dihydrotestosterone
Biochemistry, Gamma Aminobutyric Acid
Biochemistry, Glycogen
Biochemistry, Glycogenesis
Biochemistry, Glycogenolysis
Biochemistry, Hypertonicity
Biochemistry, Immunoglobulin M (IgM)
Biochemistry, Ketone Metabolism
Biochemistry, Merosin
Biochemistry, Protein Catabolism
Biochemistry, Pseudogenes
Biochemstry, Fatty Acid Oxidation
Biotin Deficiency
Bloom Syndrome (Congenital Telangiectatic Erythema)
Blue Nevus
Bone Age
Breast Milk Jaundice
Bronchial Atresia
Bronchopulmonary Dysplasia
Bruton Agammaglobulinemia
C 17 Hydroxylase Deficiency
Cafe Au Lait Macules
Calcifying Epithelioma of Malherbe (Pilomatrixoma)
Canavan Disease
Carbamazepine
Carnitine Deficiency
Cataract Surgery
Cavum Septum Pellucidum
Cavum Veli Interpositi
Central and Peripheral Cyanosis
Cerebral Palsy
CHARGE Syndrome
Chediak Higashi Syndrome
Cherry Red Spot
Chest Wall Deformities
Chiari II Malformation
Child Abuse and Neglect
Child Physical Abuse And Neglect
Child Syndrome
Choanal Atresia
Choledochal Cyst
Choroid Plexus Papilloma
Chromosome Instability Syndromes
Ciliary Dysfunction (Kartagener Syndrome, Primary Ciliary Dyskinesia)
Circumstantiality
Cleft Hand (Ectrodactyly, Split Hand)
Cleft Lip
Clinodactyly
Cloacal Malformations
Clubfoot
Cockayne Syndrome
Cognitive Development
Colic
Complement Deficiency
Complex Partial Seizure
Congenital Diaphragmatic Hernia
Congenital Hereditary Endothelial Dystrophy
Congenital Hypothyroidism
Congenital Muscular Dystrophy
Congenital Nevus
Congenital Pulmonary Airway Malformation
Congenital Rubella
Congenital Smooth Muscle Hamartoma
Congenital Syphilis
Congenital Torticollis
Constitutional Growth Delay
Coprolalia
Cor Triatriatum
Cornelia de Lange Syndrome
Coronary Arteriovenous Fistula
Coronary Artery Anomalies
Coronary Cameral Fistula
Corpus Callosum Agenesis
Craniosynostosis
Cri Du Chat Syndrome
Crigler Technique For Congenital Nasolacrimal Duct Obstruction
Crouzon Syndrome
Cryptorchidism
Cutis Verticis Gyrata
Cyanotic Heart Disease
Cystic Fibrosis
Cystic Fibrosis Related Diabetes (CFRD)
Dacryocystorhinostomy
Danon Disease
Defense Mechanisms
Delayed Hypersensitivity Reactions
Delayed Puberty
Dental Caries
Dermal Melanocytosis (Mongolian Spot), Congenital
Development Milestones
Developmental Stages of Social Emotional Development In Children
Diabetic Embryopathy
DiGeorge Syndrome
Diphtheria Tetanus Pertussis (DTaP) Vaccine
Doll's Eyes
Dornase Alfa
Double Chambered Right Ventricle
Down Syndrome (Trisomy 21)
Drowning
Duchenne Muscular Dystrophy
Duodenal Atresia And Stenosis
Dyskeratosis Congenita
Dyslexia
Dystonia
EEG, Abnormal Waveforms
Ehlers Danlos Syndrome
Electrical Status Epilepticus In Sleep (ESES)
Embryology, Atrioventricular Septum
Embryology, Central Nervous System, Malformations
Embryology, Ductus Venosus
Embryology, Ear
Embryology, Ectoderm
Embryology, Eye Malformations
Embryology, Fertilization
Embryology, Gastrulation
Embryology, Hair
Embryology, Kidney, Bladder, and Ureter
Embryology, Midgut
Embryology, Optic Fissure
Embryology, Pharyngeal Pouch
Embryology, Rectum and Anal Canal
Embryology, Sexual Development
Embryology, Testicle
Embryology, Uterus
Embryology, Vertebral Column Development
Embryology, Yolk Sac
Endocardial Fibroelastosis
Epidermal Nevus Syndromes
Epiphora Clinical Testing
Epstein Pearls
Eriksons Stages of Psychosocial Development
Eustachian Tube Dysfunction
Eyelid Coloboma
Failure To Thrive
Familial Short Stature
Fanconi Anemia
Fecal Impaction
Female Development
Fetal Alcohol Syndrome
Fifth-Toe Deformities
Fragile X Syndrome
Fructose 1-Phosphate Aldolase Deficiency (Fructose Intolerance)
Galactose 1 Phosphate Uridyltransferase Deficiency (Galactosemia)
Gastroschisis
Gaucher Disease
Genetics, Chromosome Abnormalities
Genetics, Chromosomes
Genetics, Gonadal Dysgenesis
Genetics, Mosaicism
Genetics, Somatic Mutation
Genetics, Transposons
Genetics, TREX1 Mutations
Genetics, Trinucleotide
Genetics, X-Linked Inheritance
Genu Valgum
Gerstmann Syndrome
Gigantism And Acromegaly
Glycogen Storage Disease
Glycogen Storage Disease Type I (Von Gierke Disease)
Good Samaritan Laws
Gout (Podagra)
Grasp Reflex
Gyrate Atrophy Of The Choroid and Retina
Hallervorden Spatz Disease (Pantothenate Kinase-Associated Neurodegeneration, PKAN)
Hartnup Disease
Hearing Loss
Height Assessment
Hereditary Fructose Intolerance
Herpes Simplex Encephalitis
Histology, Myelin
Histology, Osteoprogenitor Cells
Histology, Parathyroid Gland
Histology, T-Cell Lymphocyte
Holt Oram Syndrome
Horseshoe Kidney
Hurler Syndrome
Hydranencephaly
Hypercalciuria
Hyperpituitarism
Hypertrichosis
Hypokalemic Periodic Paralysis
Hypomelanosis of Ito
Hypospadias
I-123 Uptake
Ichthyosis X-Linked
Ileal Atresia
Immunodeficiency
Immunotherapy
Imperforate Anus
Inborn Errors Of Metabolism
Infant Apnea
Infantile and Juvenile Scoliosis
Infantile Cortical Hyperostosis (Caffey Disease)
Infantile Spasm (West Syndrome)
Infantile Spasms
Instrumental Activity of Daily Living (IADL)
Intellectual Disability
Interrupted Aortic Arch
Intravenous Pyelogram
Jacobs (XYY) Syndrome
Jervell and Lange Nielsen Syndrome
Job Syndrome (Hyperimmunoglobulin E)
Juvenile Absence Epilepsy
Juvenile Idiopathic Arthritis (JIA)
Juvenile Xanthogranuloma (Nevoxanthoendothelioma, JXG)
Kallmann Syndrome
Kasabach Merritt Syndrome
Kearns Sayre Syndrome
Keratoendotheliitis Fugax Hereditaria
Kernicterus
Klinefelter Syndrome
Klippel Feil Syndrome
Kyphosis
Lafora Disease
Landau Kleffner Syndrome
Laryngomalacia
Lead Toxicity
Learning Disability
Legg Calve Perthes Disease (Calves Disease)
Lennox Gastaut Syndrome
Lesch Nyhan Syndrome
Leuprolide
Lichen Nitidus
Lipemia Retinalis
Lisch Nodules
Loose Anagen Syndrome
Lymphedema
Malabsorption Syndromes
Maple Syrup Urine Disease
Marasmus
Maturity Onset Diabetes in the Young (MODY)
McCune Albright Syndrome
Meconium Ileus
Melas Syndrome
Meningomyelocele
Modified Ashworth Scale
Monilethrix
Morphea
Multidirectional Shoulder Instability (MDI)
Muscle Strength Grading
Myelomeningocele
Myers Brigg
Myotonic Dystrophy
Nail Patella Syndrome
Nasal Foreign Body
Neonatal Evaluation
Neonatal Myasthenia Gravis
Neural Tube Disorders
Neuroanatomy, Corpus Callosum
Neuroanatomy, Dentate Nucleus
Neuroanatomy, Nucleus Caudate
Neuroanatomy, Superior Sagittal Sinus
Neuroanatomy, Thalamocortical Radiations
Neurocutaneous Syndromes
Neurofibroma
Neurofibromatosis Type 1 (Von Recklinghausen)
Newborn Screening
Newborn Subcutaneous Fat Necrosis
Nicotinic Acid Deficiency (Pellagra)
Niemann-Pick Disease
Night Terrors
Nocturnal Enuresis
Nonketotic Hyperglycinemia
Noonan Syndrome
Obesity, Stigma And Discrimination
Occupational Therapy
Omphalocele
Opioid Withdrawal
Opisthotonus
Oppositional Defiant Disorder
Optic Nerve Coloboma
Ornithine Transcarbamylase Deficiency
Osteochondroma
Osteogenesis Imperfecta
Osteoma Cutis
Osteopetrosis
Otalgia
Oxygen Toxicity
Palmar Grasp Reflex
Pancreas Imaging
Patau Syndrome
Patent Ductus Arteriosus
Patent Urachus
Patient Confidentiality
Pectus Carinatum (Pigeon Chest)
Pectus Excavatum
Pediatric Bronchiolitis
Pediatric Functional Constipation
Pediatric Hearing Loss
Pediatric Obstructive Sleep Apnea
Pediatric Umbilical Hernia
Peer Play
Pendred Syndrome
Pentalogy of Cantrell
Periventricular Hemorrhage-Intraventricular Hemorrhage
Peyer Patches
Pfeiffer Syndrome
PHACE Syndrome
Phenylketonuria
Phenytoin
Phocomelia
Physiology, Cellular Receptor
Physiology, Fetal Circulation
Physiology, Gastrocolic Reflex (Gastrocolic Response)
Physiology, Gonadotropin Inhibitor
Physiology, Gonadotropin-Releasing Hormone (GnRH)
Physiology, Krebs Cycle
Physiology, Long Term Memory
Physiology, Male Reproductive System
Physiology, Membrane
Physiology, Menstrual Cycle
Physiology, Muscle
Physiology, Parathyroid
Physiology, Proteins
Physiology, Puberty
Physiology, Sexual Maturity Rating
Physiology, Testosterone
Piaget
Piebaldism
Poikiloderma Congenitale
Poland Syndrome
Polycystic Ovarian Disease (Stein-Leventhal Syndrome)
Polyglandular Autoimmune Syndrome Type I
Polyglandular Autoimmune Syndrome, Type II (Carpenters, Schmidt)
Prader-Willi Syndrome
Precocious Puberty
Pregnancy
Prenatal Genetic Screening
Preterm Labor
Primary Amenorrhea
Primitive Reflexes
Procaine Penicillin
Progressive Familial Intrahepatic Cholestasis (Byler Disease)
Protected Health Information (PHI)
Prune Belly Syndrome
Pseudohypoparathyroidism
Pulmonary Sequestration
Pure Red Cell Aplasia
Radial Dysplasia (Clubhand)
Rapid Eye Movement Sleep Behavior Disorder
Red Reflex
Renal Cyst
Rett Syndrome
Right Aortic Arches
Rolandic Epilepsy (BRE) Seizure
Rooting Reflex
Routine Newborn Care
Sandifer Syndrome
Scheuermann Disease
Scleredema (Buschke Disease, Scleredema of Buschke, Scleredema Adultorum)
Sensory Integration
Severe Combined Immunodeficiency
Short Stature
Single Ventricle
Sinus Tachycardia
Spasticity
Special Education
Speech Assessment
Spina Bifida
Spinal Dysraphism And Myelomeningocele
Spinocerebellar Ataxia
Sports Physicals
Steatorrhea
Stereognosis
Sternoclavicular Joint Injury
Stimulants
Sturge-Weber Syndrome
Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome)
Subaortic Stenosis
Suicide Risk
Supravalvar Aortic Stenosis (SVAS)
Surfactant
Swyer-James-MacLeod Syndrome
Syndactyly
Syndromic Sensorineural Hearing Loss (SSHL)
Syringomyelia
Talipes Equinovarus
Tanner Stages
Temper Tantrums
Teratogenic Medications
Tetanus Toxoid
Tetralogy of Fallot
Thalassemia
Thoracic Aorta Aneurysm
Thumb Sucking
Thyroxine-Binding Globulin Deficiency
Tonsillitis
Tort
Torticollis
Tourette Syndrome And Other Tic Disorders
Tracheoesophageal Fistula
Tracheomalacia
Trinucleotide Repeat Disorders
Trisomy 13
Truncus Arteriosus
Tuberous Sclerosis
Turner Syndrome
Urea Cycle Disorders
Vaginal Foreign Body Evaluation and Treatment
Vascular Ring Double Aortic Arch
Velocardiofacial Syndrome
Vernix Caseosa
Vigabatrin
Vitamin E
Vitamin K Deficiency
Vohwinkel Syndrome
Weibel Palade Bodies
Werdnig Hoffmann Disease
Williams Syndrome
Wilson Disease
Wiskott-Aldrich Syndrome
Wyburn-Mason Syndrome
X-linked Agammaglobulinemia