3/31-4/4

Monday	-Overview notes on Human Body Systems and Functions -Skeletal System ppt
Tuesday	-PARCC -Muscular System ppt
Wednesday	-Quiz on Body Systems/Functions and Medical Terminology -Integumentary System ppt
Thursday	-Activity/Lab
Friday	-Nutrition/Digestive System ppt

3/17-3/21

Monday	-Thompson Family Fortune Pedigree Project -Study guide for Chapter 5 Test -Genetic Disorder Project due on Thursday, 3/20
Tuesday	-Continue to work on Thompson Family Fortune
Wednesday	-Review for Chapter 5 Test -Finish Thompson Family Fortune
Thursday	-Genetic Disorder Project due today -Oral presentations begin
Friday	-Chapter 5 Test today -Oral presentations

Genetic Disorder Project Note-taking Guide

Name ________________________________ Block ________

Heredity and Genetic Disease Research Report Note-taking Guide

Use the following note-taking guide to help you take down important information regarding your topic.  This will serves as a checklist to make sure that you’ve gathered all of the necessary information and should help you summarize the information in your own words.

Section A:  Description of the genetic disorder/condition?

1.  Where does the name come from or what does it mean? _______________________________________________________________

_______________________________________________________________

citation:  ______________________________________________________________________

2a.  When was it discovered? _____________________________________________________

citation:  ______________________________________________________________________

2b.  How was it discovered? ______________________________________________________

citation:  ______________________________________________________________________

2c.  Who discovered it?  _________________________________________________________

citation:  ______________________________________________________________________

2d.  Where was it first seen?  _____________________________________________________

citation:  ______________________________________________________________________

3a.  What are the signs and/or symptoms of the disorder?  ______________________________

citation:  ______________________________________________________________________

Section B:  Percent of population/probability of births (use statistics)

1a.  How many children are born with this disorder?  ___________________________________

citation:  ______________________________________________________________________

1b.  How often does the disorder occur?  ____________________________________________

citation:  ______________________________________________________________________

1c.  How rare is the disorder?  _____________________________________________________

citation:  ______________________________________________________________________

2a.  Does it occur in males more often or in females more often?  _________________________

citation:  ______________________________________________________________________

2b.  What is the male to female ratio ________________________________________________

citation:  ______________________________________________________________________

Section C:  Inheritance Patterns

1a.  How is the disorder inherited?  _________________________________________________

citation:  ______________________________________________________________________

1b.  What type of disorder is it?  (chromosomal, protein deficiency, enzyme deficiency, sex-linked, recessive)  ___________________________________________________________

citation:  ______________________________________________________________________

Section D:  Treatments

1a.  What are the treatments, if any? ________________________________________________

citation:  ______________________________________________________________________

1b.  Are there any medications available? If yes, what are they?  ______________________________________________________________________

______________________________________________________________________

citation:  ______________________________________________________________________

Section E:  Life Expectancy

1a.  How long do people with the disorder live?  _______________________________________

citation:  ______________________________________________________________________

1b.  What is everyday life like for a person with this disorder?  ______________________________________________________________________

______________________________________________________________________

citation:  ______________________________________________________________________

Section F:  Organizations/Foundations/Resources

1.  What organizations/foundations or resources are available to help the families?  

______________________________________________________________________

citation:  ______________________________________________________________________

Section G:  Citations and documentations

1a.  How many pictures have you included in your project folder?  ________________________

1b.  How many diagrams have you included in your project folder?  _______________________

1c.  How many tables and/or charts have you included in your project folder?  _______________________

2.  Which citation website did you use?_______________________________

Timeline to help you stay on track with your project:

Amazing Stories!

Genetic Disorder Project

Genetic Disorders Name

Achondroplasia(Dwarfism)
Achromatopsia
Acid Maltase Syndrome/Pompe’s Disorder
Acromegaly/Gigantism
Adrenoleukodystrophy/Lorenzo’s Oil
Aicardi Syndrome
Albinism
Angelman Syndrome
Alkaptonuria
Alpha-1 Antitrypsin Deficiency
Amyotrophic Lateral Sclerosis(ALS)
Androgen Insensitivity Syndrome
Arrhythmogenic Right Ventricular Dysplasia
Apert Syndrome
Asperger Syndrome/Autism
Ataxia Telangiectasia
Barth Syndrome
Bloom Syndrome
Blue Rubber Bleb Nevus Syndrome
Canavan Disease

Celiac Disease
CHARGE Syndrome
CIPA (Congenital Insensitivity to Pain w/ Anhidrosis)
Coffin-Lowry Syndrome
Corpus Callosum Agenesis
Cri-Du-Chat Syndrome
Crohn’s Disease
Cystic Fibrosis
Cystinosis
Dercum’s Disease
Down Syndrome/Trisomy 21
Duchenne’s Muscular Dystrophy
Ectodermal Dysplasia
Edward’s Syndrome/Trisomy 18
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Epilepsy
Factor V Leiden Thrombophilia
Fanconi Anemia
Fibrodysplasia Ossificans Progressiva

Fragile X Syndrome
Galactosemia
Gaucher Disease
Hemochromatosis
Hemophilia
Huntington’s Disease
Hurler Syndrome
Hypophosphatasia
Ichthyosis
Klinefelter Syndrome/XXY
Krabbes Disease
Langer-Giedion Syndrome
Leukodystrophy
Long QT Syndrome
Marfan Syndrome
Moebius Syndrome
Mucopolysaccharidosis
Multiple Sclerosis
Myotonic Dystrophy
Nail-Patella Syndrome/Fong Syndrome

Nephrogenic Diabetes Insipidus
Neurofibromatosis
Niemann-Pick Disease
Osteogenesis Imperfecta
Patau Syndrome/Trisomy 13
Phenylketonuria (PKU)
Porphyrias
Prader-Willi Syndrome
Progeria Syndrome
Proteus Syndrome
Prune-belly Syndrome
Retinoblastoma (Eye Cancer)
Rett Syndrome Rubinstein-Taybi Syndrome
Sanfilippo Syndrome
Schwachmann Syndrome
Severe Combined Immuno Deficiency Syndrome (SCID)
Sickle Cell Disease
Sirenomelia
Smith-Magenis Syndrome
Stickler Syndrome

Tay-Sachs Disease
Treacher Collins Syndrome
Tuberous Sclerosis
Turner Syndrome
Urea Cycle Disorder
Usher Syndrome
Vitiligo
Von Hippel-Lindau Syndrome
Waardenberg Syndrome
Werner’s Syndrome
Williams Syndrome
Wilson’s Disease
Xeroderma Pigmentosum
Super Male/XYY Syndrome
Methemoglobinemia
Tree man