Advanced Pediatric Genetic Disorders
( 25 Modules )

Module #1
Introduction to Pediatric Genetic Disorders
Overview of genetic disorders in pediatrics, importance of genetic testing, and current trends in the field.

Module #2
Genetics 101:Fundamentals and Terminology
Review of basic genetic principles, including DNA structure, gene expression, and inheritance patterns.

Module #3
Pediatric Genetic Syndromes:Overview and Classification
Classification of pediatric genetic syndromes, including chromosomal abnormalities, single-gene disorders, and complex traits.

Module #4
Chromosomal Abnormalities:Diagnosis and Management
In-depth discussion of chromosomal abnormalities, including Down syndrome, Turner syndrome, and Klinefelter syndrome.

Module #5
Single-Gene Disorders:Autosomal Dominant and Recessive Traits
Analysis of single-gene disorders, including Marfan syndrome, sickle cell disease, and cystic fibrosis.

Module #6
X-Linked Disorders:Hemophilia and Muscular Dystrophy
In-depth discussion of X-linked disorders, including hemophilia A and B, and Duchenne muscular dystrophy.

Module #7
Mitochondrial Disorders:Diagnosis and Management
Overview of mitochondrial disorders, including Leigh syndrome, MELAS, and Kearns-Sayre syndrome.

Module #8
Genetic Testing:Types, Interpretation, and Limitations
Discussion of various genetic testing methods, including karyotyping, molecular testing, and next-generation sequencing.

Module #9
Prenatal Genetic Testing:Options and Ethics
Overview of prenatal genetic testing, including non-invasive prenatal testing (NIPT), chorionic villus sampling (CVS), and amniocentesis.

Module #10
Genetic Counseling:Principles and Practice
Introduction to genetic counseling, including communication strategies, risk assessment, and family history taking.

Module #11
Neurodevelopmental Disorders:Genetics and Management
Analysis of neurodevelopmental disorders, including autism spectrum disorder, ADHD, and intellectual disability.

Module #12
Metabolic Disorders:Inborn Errors of Metabolism
In-depth discussion of inborn errors of metabolism, including phenylketonuria, maple syrup urine disease, and galactosemia.

Module #13
Cancer Genetics:Pediatric Oncology and Hereditary Cancer Syndromes
Overview of pediatric cancer genetics, including retinoblastoma, neurofibromatosis type 1, and Li-Fraumeni syndrome.

Module #14
Cardiovascular Genetics:Congenital Heart Defects and Hereditary Cardiovascular Disorders
Analysis of cardiovascular genetics, including congenital heart defects, hypertrophic cardiomyopathy, and familial hypercholesterolemia.

Module #15
Genetic Dermatological Disorders:Skin and Hair Abnormalities
In-depth discussion of genetic dermatological disorders, including epidermolysis bullosa, ichthyosis, and ectodermal dysplasias.

Module #16
Ophthalmic Genetics:Eye Abnormalities and Vision Loss
Overview of ophthalmic genetics, including cataracts, glaucoma, and Leber congenital amaurosis.

Module #17
Audiovestibular Genetics:Hearing Loss and Balance Disorders
Analysis of audiovestibular genetics, including sensorineural hearing loss, otosclerosis, and vestibular migraine.

Module #18
Immunological Genetics:Primary Immunodeficiency Disorders
In-depth discussion of primary immunodeficiency disorders, including severe combined immunodeficiency, Brutons agammaglobulinemia, and chronic granulomatous disease.

Module #19
Gastrointestinal Genetics:Gastrointestinal Disorders and Nutritional Deficiencies
Overview of gastrointestinal genetics, including short gut syndrome, Crohns disease, and celiac disease.

Module #20
Musculoskeletal Genetics:Muscular Dystrophies and Skeletal Dysplasias
Analysis of musculoskeletal genetics, including Duchenne muscular dystrophy, Becker muscular dystrophy, and osteogenesis imperfecta.

Module #21
Neuromuscular Genetics:Neuropathies and Myopathies
In-depth discussion of neuromuscular genetics, including Charcot-Marie-Tooth disease, spinal muscular atrophy, and myotonic dystrophy.

Module #22
Renal Genetics:Kidney Diseases and Abnormalities
Overview of renal genetics, including polycystic kidney disease, Alport syndrome, and congenital anomalies of the kidney and urinary tract.

Module #23
Respiratory Genetics:Pulmonary Disorders and Respiratory Failure
Analysis of respiratory genetics, including cystic fibrosis, alpha-1 antitrypsin deficiency, and surfactant protein deficiencies.

Module #24
Endocrine Genetics:Hormone Disorders and Endocrine Abnormalities
In-depth discussion of endocrine genetics, including congenital adrenal hyperplasia, thyroid disease, and growth hormone deficiency.

Module #25
Course Wrap-Up & Conclusion
Planning next steps in Advanced Pediatric Genetic Disorders career

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Advanced Pediatric Genetic Disorders ( 25 Modules )

Advanced Pediatric Genetic Disorders
( 25 Modules )