GENERAL PAEDIATRICS
2015/2016
2019/2020
DM270
MED/38 (PEDIATRIA GENERALE E SPECIALISTICA)
DIPARTIMENTO DI MEDICINA MOLECOLARE
MEDICINA E CHIRURGIA (IN LINGUA INGLESE)
PERCORSO COMUNE
PRIMO SEMESTRE (01/10/2019 - 17/01/2020)
5
40 ore di attività frontale
English
ORALE
CALCATERRA VALERIA - 1 CFU
COMOLI PATRIZIA ELSA - 1 CFU
LICARI AMELIA - 3 CFU
Neonatology
Physical examination of the newborn, infant jaundice and hyperbilirubinemia in the newborn, neonatal necrotizing enterocolitis, hyaline membrane disease, retinopathy of prematurity, intracranial-intraventricular hemorrhage and periventricular leukomalacia,

Endocrinological disorders
Type 1 and 2 diabetes mellitus and other specific types of diabetes (MODY, neonatal diabetes), diabetes insipidus, obesity and metabolic syndrome, precocious/delayed puberty, hypothyroidism, hyperthiroidism, thyroid nodules, neoplasia of the thyroid, congenital adrenal hyperplasia, disorders of sex development

Cardiovascular System
Fetal-neonatal and transitional circulation, congenital heart malformations

Respiratory disorders
Bronchiolitis, Community-Acquired Pneumonia, Asthma

Gastrointestinal Diseases
Hypertrophic pyloric stenosis, inflammatory bowel disease (chronic ulcerative colitis, Crohn disease, celiac disease).

Rheumatic Diseases
Rheumatic disease, juvenile idiopathic arthritis, systemic lupus erythematosus, Kawasaki disease, Henoch-Schönlein purpura, rheumatic fever

Nephro-urological diseases
Urinary Tract Infections, Glomerulonephritis, Nephrotic Syndrome

Neurological disorders
Febrile seizures, acute bacterial meningitis, viral meningoencephalitis

Infectious diseases
Measles, Rubella, Mumps, Varicella-Zoster Virus Infections, Epstein-Barr Virus

Hematological diseases
Immunodeficiency, anemias, thalassemia syndromes, leukemias, thrombocytopenia, lymphoma, histiocytosis syndromes, Wilms tumor, neuroblastoma

Genetic syndromes
S. Klynefetler, S. Turner, S. Down, S. Prader Willi.
Nelson TextBook of Pediatrics