Petter Khant MF4 Neurology
Activity
Tutorial
Tutorial
Petter Khant, a 6-year-old boy, is brought to his family doctor by his mother because of concerns that he is not learning in school. He is described as a "high energy child", always on the go. He has a very short attention span. His teacher sent along a note explaining that Petter is well behind the expectations for this age. His classmates are learning the sounds that go with different letters, but Petter does not yet even have a concept of letters or numbers. His vocabulary seems very limited, both receptive and expressive. His mother recalls no concerns about his early development. She remembers him as a generally healthy baby. He started to crawl at 9 months and could walk on his own by 13 months. He only began to use a few single words at 2 years of age. A hearing test done at that time was normal.
Curriculum Block
Medical Foundation 4 / Neuroscience / Part 4 / Week 3
- Indicates most relevant
Objectives
General Objectives
- Recall major normal neurodevelopmental milestones in child development.
- Review the genetic concept of trinucleotide repeats and anticipation.
- Define “developmental delay”.
Global Objectives
Assessments
End-Unit Tutorial Assessment
Mini Concept Application Exercise (CAE)
Tags
AFMC National Clinical Skills
Neurological Examination
Basic Sciences
Biochemistry
Genetics
Human development
Cohort Year
2010
Curriculum Block
Medical Foundation 4
Neuroscience
Part 4
Week 3
Curriculum Week
Part 4
Week 7
Discipline
Family medicine
Genetics
Neurology
Pediatrics
MCC Presentations
Congenital Anomalies, Dysmorphic Features
Developmental Delay
Language and Speech Disorders
McMaster Program Competencies
2.2 Apply biomedical scientific principles fundamental to health care for patients and populations.
2.3 Apply principles of clinical sciences to diagnostic and therapeutic decision-making, clinical problem-solving, and other aspects of evidence-based healthcare
MeSH
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Craniofacial Abnormalities [C05.660.207]
Child Development [G07.345.374.750]
Child [M01.060.406]
Epigenesis, Genetic [G05.355.315.203]
Fragile X Syndrome [C10.597.606.643.455.500]
Funnel Chest [C05.660.386]
Gene Expression Regulation [G05.355.315]
Growth and Development [G07.345]
Hematologic Tests [E01.370.225.625]
Hyperkinesis [C10.597.350.350]
Mental Retardation, X-Linked [C10.597.606.643.455]
Neurobehavioral Manifestations [C10.597.606]
Neurologic Manifestations [C10.597]
Pediatrics [H02.403.670]
Sex Chromosome Disorders [C16.131.260.800]
Trinucleotide Repeat Expansion [G05.355.600.220.865]
X Chromosome Inactivation [G05.355.315.203.249.970]