Russian Association of Pediatricians: Clinical Guidelines
85 guidelines developed with the participation of the Russian Association of Pediatricians.
- X-linked adrenoleukodystrophy
- Allergic rhinitis
- Congenital aniridia
- Atopic dermatitis
- Maple syrup urine disease
- Crohn's disease
- Niemann-Pick disease type C
- Pompe disease
- Fabry disease
- Bronchial asthma
- Bronchitis
- Bronchopulmonary dysplasia
- Congenital pneumonia
- Congenital epidermolysis bullosa
- Gastritis and duodenitis in children
- Gastro-esophageal reflux disease in children
- Hemolytic uremic syndrome
- Glomerular diseases: Immunoglobulin A nephropathy
- Glutaric aciduria type 1
- Contact dermatitis
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
- Other disorders of branched-chain amino acid metabolism (Methylmalonic acidemia/aciduria)
- Other inflammatory polyneuropathies (Chronic inflammatory demyelinating polyradiculoneuropathy)
- Other hepatitis
- Other lipid storage disorders (Lysosomal acid lipase deficiency)
- Other sphingolipidoses (Gaucher disease)
- Other sphingolipidoses (Niemann-Pick disease types A, B, A/B)
- Other specified congenital anomalies of respiratory system (Primary ciliary dyskinesia)
- Cholelithiasis
- Isovaleric acidemia/aciduria
- Urinary tract infection
- Renal cyst in children
- Cystic fibrosis
- Classical phenylketonuria and other hyperphenylalaninemias
- Cutaneous horn
- Urticaria
- Pulmonary hypertension in children
- Metabolic dysfunction-associated steatotic liver disease in children
- Multiple carboxylase deficiency (Biotinidase and holocarboxylase synthetase deficiencies)
- Corns and callosities
- Urolithiasis
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type I
- Mucopolysaccharidosis type II
- Mucopolysaccharidosis type II
- Mucopolysaccharidosis type VI
- Mucopolysaccharidosis type VI
- Otitis externa
- Disorders of sulfur-bearing amino acid metabolism (Homocystinuria)
- Phosphorus metabolism disorders (Hypophosphatasia)
- Disorders of mitochondrial fatty acid $\beta$-oxidation
- Galactose metabolism disorders (Galactosemia)
- Copper metabolism disorders (Wilson disease)
- Hereditary tyrosinemia type 1
- Hereditary angioedema
- 3-Methylcrotonyl-CoA carboxylase deficiency (3-methylcrotonylglycinuria, methylcrotonyl-CoA carboxylase deficiency)
- Vitamin D deficiency. Rickets.
- Mitochondrial acetoacetyl-CoA thiolase deficiency ($\beta$-ketothiolase deficiency, T2 deficiency)
- Malnutrition in children older than 1 year (Protein-energy malnutrition)
- Sensorineural hearing loss in children
- Acute respiratory viral infection (ARVI)
- Acute bronchiolitis
- Acute laryngitis
- Acute obstructive laryngitis [croup], epiglottitis, post-intubation laryngeal edema
- Acute tonsillitis and pharyngitis (Acute tonsillopharyngitis)
- Food Allergy
- Pneumonia (community-acquired)
- Acquired keratosis (keratoderma) of palm and sole
- Duchenne progressive muscular dystrophy. Becker progressive muscular dystrophy
- Pressure ulcer
- Propionic acidemia/aciduria
- Autism spectrum disorders
- Seborrheic keratosis
- Glut1 deficiency syndrome
- Teething syndrome (primary teeth)
- Irritable bowel syndrome
- Functional dyspepsia in children
- Chemical burn of esophagus
- Chronic kidney disease
- Celiac disease
- Enuresis
- Eosinophilic esophagitis
- Erythemas
- Peptic ulcer of the stomach and/or duodenum
- Ulcerative colitis
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