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- Pediatric Legionnaires Nephropathy
- Pediatric glycogen storage disease type III
- Pediatric glycogen storage disease type Ⅵ
- Proximal renal tubular acidosis in children
- Pediatric glycogen storage disease type
- Congenital agammaglobulinemia
- Lacunar cerebral infarction
- Breast nodule
- Autoimmune liver disease
- Striated hypertrophy of limbs
- Post-steroidal panniculitis
- Colorado tick fever
- Acquired cyclic anticoagulant syndrome
- Anterior spinal cord syndrome
- Orbital amyloidosis
- Congenital esophageal duplication
- Vascular headache
- Gittling syndrome
- Pediatric Mediastinal Compression Syndrome
- Calcification of prostate
- Pyrimethamine poisoning
- Left varicocele
- Pediatric hemorrhagic shock and encephalopathy syndrome
- Orbital meninges-encephalocele
- Red bean
- Congenital bowel rotation abnormalities
- Secondary monoclonal immunoglobulin disease
- Congenital giant urethra
- Methotrexate-related lymphoproliferative disease
- Pediatric purine nucleotide phosphorylase deficiency
- Lafora disease
- Adrenal tumor
- Plantar fasciitis
- Pediatric Listeria
- Pediatric serum disease
- Traumatic bile duct injury
- Non-firearm open brain injury
- Pediatric glycogen storage disease type Ⅱ
- Choroidal atrophy
- Heterotopic renal vessels and accessory vessels
- Congenital anterior urethral valve
- Pediatric pyramidal dysfunction syndrome
- Intraesophageal diverticulum
- Alpha1-antitrypsin deficiency in children
- Spinal anterior central artery ischemic syndrome
- Niznov syndrome
- Cotton seed poisoning
- Myeloperoxidase deficiency
- Scorpion sting
- Posterior spinal artery ischemia syndrome
- Neonatal renal venous thrombosis
- Single episode depression
- Claudication choroiditis
- Capsular histoplasmosis
- Pyrimidine 5′-nucleotide deficiency
- Pediatric Tropical Giant Spleen Syndrome
- Congenital stenosis and atresia
- Small omental hernia
- Pediatric yaws
- Transvestite
- Pediatric total distal tubular acidosis
- Anti-activated protein C
- Mucopolysaccharidosis in children
- Pediatric Ebola virus disease
- Primary segmental infarction
- Skin diseases caused by antimony and its compounds
- Pediatric low cardiac output syndrome
- Spinal cord firearm injury
- Spontaneous rupture of rectus abdominis
- Post-transplant lymphoproliferative disease
- Striatum
- Orbital hemangiopericytoma
- Spontaneous retroperitoneal hemorrhage or hematoma
- Pediatric Unilateral Lung Abnormal Translucent Syndrome
- Proctitis
- Pediatric Niemann-Pick disease
- Hexokinase deficiency
- Intrathoracic kidney
- Renal damage in primary macroglobulinemia
- Empty saddle syndrome in children
- Epidural and subdural abscesses
- Hereditary factor Ⅶ deficiency
- Myelopathy due to electric shock
- Disseminated intravascular coagulation in children
- Spinal cord injury
- Hepatoma and rupture during pregnancy
- Internal hernia
- Mucopolysaccharidosis type Ⅶ
- Pediatric osteosclerosis
- Inflammatory bowel disease
- Pediatric Cooking Syndrome
- Pediatric jaksh syndrome
- Pediatric dialysis imbalance syndrome
- Neonatal transient pustular melanosis
- Pediatric desquamative pneumonia
- Filariasis
- Acute intermittent porphyria in children
- Atypical mycobacterial scleritis
- Pediatric phosphatase
- Fibrochondroma
- Pediatric Echo and Coxsackie virus infection
- Orbital osteomyelitis
- Pediatric cast syndrome
- Chorea of pregnancy
- Hemoglobinemia
- Pediatric contusion and laceration
- Budd-Gialy syndrome
- Congenital bladder neck contracture
- Streptococcus mie pneumonia
- Visceral larval migration in children
- Tricuspid valve malformation
- Metallic discoloration
- Pediatric aquatic histiocytosis
- Throwing sport
- Sezeri syndrome
- Retroperitoneal fluid leakage
- Epidural abscess
- Progressive Backbone Dysplasia
- Non-lipid reticular endothelial proliferation syndrome in children
- Esophageal repetitive deformity
- Mycobacterium infection
- Congenital absent tibia
- Osteocystis
- Pigmented paravenous retinal choroidal atrophy
- Blastomycosis
- Pediatric drug-induced hemolytic anemia
- Congenital photosensitivity porphyria in children
- Pre-pediatric contraction
- Vertebral arch tuberculosis
- Pediatric other salmonella infections
- Retroperitoneal hemorrhage
- Paroxysmal ventricular tachycardia in children
- Infantile cortical hyperplasia
- Pediatric salicylate poisoning
- Genital warts
- Dental tumor
- Westcott-Aldrich syndrome
- Aeromonas pneumonia
- Lymphoproliferative disease associated with primary immune disease
- Giardiasis in children
- Pregnancy with urolithiasis
- Optic beam lesions
- Pulmonary blastomycosis
- Skin diseases caused by beryllium and its compounds
- Primary cutaneous immune cell tumor
- Hereditary protein C deficiency
- Root artery ischemia syndrome supplying blood to cervical spinal cord
- Ectopic and dislocation of crystals
- Congenital sensory neuropathy
- Pediatric acute bloodborne osteomyelitis
- Tibia and fibula joint anterior separation
- Multiple epiphyseal dysplasia
- Retrocranial fossa meningioma in children
- Trichosporiasis
- Dysfunction of platelet release in children
- Orbital knockout fracture
- Absent urethra and congenital atresia
- Giant spiny echinococcosis
- Malignant chondrogenic syringoma
- Niacin deficiency neuropathy
- Hypochlorite azotemia syndrome in children
- Hematoporphyrinic peripheral neuropathy
- Rickettsia rickii
- Bladder agenesis and hypoplasia
- Pediatric disseminated lipogranuloma syndrome
- Amyloidosis and amyloid arthropathy
- Chest actinomycosis
- Renal damage
- Loboblastomycosis
- Enterocytopathic human orphan virus infection
- Multiple hairy sheath tumors in Colden disease
- Hereditary abnormal fibrinogenemia
- Pediatric antiphospholipid syndrome
- Francis pneumonia
- Niacin deficiency in children
- Primary mediastinal infection
- Tropical pulmonary eosinophilic pneumonia
- Acute and subacute subdural hematoma
- Myxovalvular disease in the elderly
- Multi-source atrial tachycardia in children
- Pediatric Ewing sarcoma
- Painful bruising syndrome
- Pediatric lymphoid polyps
- Pediatric inferior vena cava obstruction syndrome
- Algae
- Pediatric atrial flutter
- Lang-Ower syndrome
- Gillian-Barre syndrome in children
- Pediatric asthma muscular atrophy syndrome
- Pediatric Castchin-Beck disease
- Pediatric vascular hemophilia
- Electric shock and lightning in children
- Punctate epiphysis dysplasia
- Wound botulism
- Pediatric atrial tachycardia
- Pheochromocytoma in children
- Pediatric interferon-gamma receptor deficiency
- Crude cottonseed oil poisoning
- Primary mesenteric tumor
- Pediatric torsional ventricular tachycardia
- Gaucher disease in children
- Newborn Wilson-Mikity Syndrome
- Hereditary factor Ⅴ deficiency
- Fucosin storage disease
- Pediatric tussah encephalopathy syndrome
- Pelvic hernia
- Cross ectopic kidney with or without fusion
- Congenital clavicle pseudoarticular
- Delta storage disease
- Non-occlusive mesenteric vascular ischemia
- Glucose phosphate isomerase deficiency
- Periodic normal blood potassium paralysis in children
- Choroid disease
- Pediatric unicompartmental bone cyst
- Periodic hyperkalemia in children
- Histiocytic pancreatitis
- Hereditary protein S deficiency
- Pediatric brain abscess
- Eye swine cysticercosis
- Pediatric giant platelet syndrome
- Severe acute respiratory syndrome in children
- Radial neck fracture and radial skull ridge separation
- Eye sore chemical injury
- Tuberculous keratopathy
- Osteoporosis
- Pediatric vasopressin hypersecretion syndrome
- Osteosarcoma
- Filamentous warts
- Renal Diabetes in Children
- Rickettsia siberiani
- Neglect
- Pediatric epidural hematoma
- Pediatric viral hepatitis
- Pharyngeal mechanical trauma
- Congenital gastric wall muscular defect
- Reticulosarcoma
- Pediatric schistosomiasis
- Dubo histoplasmosis
- Congenital small throat
- Hand-Schuler-Kessing disease
- Congenital dislocation of shoulder
- Pediatric arteritis
- Mucopolysaccharidosis in children type Ⅳ
- Schistosomiasis
- Pediatric cystine disease
- Hereditary fibrinogen deficiency
- Pediatric aneurysmal bone cyst
- Globinogenic anemia retinopathy
- Ciliary body melanoma
- Retrocranial fossa hematoma
- Neonatal gastrointestinal duplication
- Pediatric astrocytoma
- Ileocecal syndrome
- Kansas Mycobacterium infection
- Pediatric Eller-Donlow Syndrome
- Clear cell acanthoma
- Idiopathic delayed immunoglobulin deficiency
- Heterochromic iridocyclitis
- Cane pneumoconiosis
- Idiopathic ventricular tachycardia in children
- Pediatric facial and shoulder brachial muscular dystrophy
- Traumatic brain abscess
- Paraduodenal hernia
- Infant botulism syndrome
- Water pain
- Lunar osteochondrosis
- Synovitis of the knee
- Skin diseases caused by vanadium and its compounds
- Secondary mediastinal infection
- Pediatric Merkel diverticulum
- Epiphyseal punctate dysplasia
- Persistent pulmonary eosinophil infiltration
- Acute subdural hematoma
- Paraneoplastic myelopathy
- Pediatric pulmonary embolism
- Pediatric short finger-globular ectopic syndrome
- Pelvic floor peritoneal hernia
- Skin diseases caused by arsenic and its compounds
- Orbital subperiosteal abscess
- Acquired retinal aortic aneurysm
- Neonatal air leak
- Fifth day syndrome
- Nelson syndrome
- Congenital self-healing Langerhans histiocytosis
- Bone angioepithelial cell tumor
- Pediatric galactosemia
- Extraocular muscle extensive fibrosis syndrome
- Juvenile chronic arthritis and its associated uveitis
- Pediatric hereditary fructose intolerance
- Osteoarthropathy of pine caterpillar disease
- Corneal ulcer
- Lost stray window
- Pediatric amyloidosis
- Renal amyloidosis in children
- Hypernatremia in the elderly
- Dissipative delayed pneumonia
- Lame perforating elastic tissue degeneration
- Enter 袢 syndrome
- Hemoglobin M disease
- Esophageal webs and rings