Early Influences on Development - Prenatal Development Flashcards

1
Q

Prenatal Development

list the 3 periods, 3 trimesters, & timeframes for prenatal development

A

periods
1) germinal period: conception to end of the 2nd week
2) embryonic period: 3 to 8 weeks
3) fetal period: week 9 through birth

trimesters
1) first trimester: week 1 to week 13
2) second trimester: week 14 to week 27
3) third trimester: week 28 through birth

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2
Q

Prenatal Development

characteristics of the germinal period

A
  • zygote impants in the uterine wall
  • exposure to toxic chemicals, drugs, or other teratogens typically have an “all-or-none” effect
    • meaning that if exposure causes significant damage, implantation will not occur
    • if implantation occurs, it suggests that exposure had little to no effect
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3
Q

Prenatal Development

characteristics of the embryonic period

A
  • major organs & structures are forming
  • exposure to teratogens is most likely to cause major defects
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4
Q

Prenatal Development

characteristics of the fetal period

A
  • major organs & structures grow and msture
  • exposure to teratogens is most likely to cause minor defects or abnormalities
  • an exception is the central nervous system, which is susceptible to major damage from teratogens during both the embryonic & fetal periods
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5
Q

Prenatal Development

____ is the earliest age at which a premature baby can survive outside the womb and occurs between ____ and ____ weeks.

A

viability; 22 adn 26 weeks

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6
Q

Chromosomal Abnormalities

define & list 3 disorders due to a chromosomal deletion

A

a change in chromosome structure that involves the loss of one or more segments of a chromosome

  1. Prader-Willi Syndrome
  2. Angelman Syndrome
  3. Cri-Du-Chat Syndrome
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7
Q

Chromosomal Abnormalities

Prader-Willi
1. caused by a deletion on what chromosome
2. symptoms

A
  1. paternal chromosome 15
  2. symptoms include:
    * narrow forehead
    * almond-shaped eyes
    * short statue
    * small hands & feet
    * poor muscle tone (hypotonia)
    * global developmental delays
    * chronic overeating (hyperphagia)
    * obesity
    * hypogonadism
    * intellectual disabilities
    * skin-picking & other self-injurious behaviors
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8
Q

Chromosomal Abnormalities

Angelman Syndrome
1. due to deletion on what chromosome
2. symtoms

A
  1. maternal chromosome 15
  2. symptoms include:
    * small head & brain (microcephaly)
    * wide jaw & pointed chin
    * severe developmental delays
    * communication & intellectual disabilities
    * hyperactivity
    * tendency to be unhappy
    * ataxia
    * seizures
    * hand-flapping
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9
Q

Chromosomal Abnormalities

Cri-Du-Chat Syndrome
1. due to a deletion of what chromosome
2. symptoms

A
  1. chromosome 5
  2. symptoms range from mild to severe depending on the extent & location of the deletion & include:
    * high-pitched (cat-like) cry
    * low birth weight
    * weak muscle tone
    * characteristic facial features - widely set eyes, low-set ears, round face)
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10
Q

Chromosomal Abnormalities

list the 3 chromosomal disorders that are due to sex chromosome abnormalities

A
  1. Klinefelter Syndrome
  2. Turner Syndrome
  3. Rett Syndrome
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11
Q

Chromosomal Abnormalities

Klinefelter Syndrome
1. due to what chromosomal abnormality
2. effects males or females
3. symptoms

A
  1. the presence of 2 or more X chromosomes and a single Y chromosome
  2. males
  3. develop normal male identitiy but incomplete secondary sex characteristics and symptoms include:
    • breast enlargement (gynecomastia)
    • low testosterone
    • disproportionately long arms & legs
    • taller than normal
    • delays in language development
    • learning disabilities
    • impaired problem-solving & social skills
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12
Q

Chromosomal Abnormalities

Turner Syndrome
1. due to what chromosomal abnormality
2. effects males or females
3. symptoms

A
  1. partial or complete deletion of one of the X chromosomes
  2. females
  3. don’t develop secondary sex characteristics & are infertile; symptoms include:
    * short stature
    * stubby fingers
    * drooping eyelids
    * receding or small lower jaw
    * web-like neck
    * learning disabilities
    * heart defects
    * kidney & urinary tract abnormalities
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13
Q

Chromosomal Abnormalities

Rett Syndrome
1. due to what chromosomal abnormality
2. effects males or females
3. symptoms

A
  1. X-linked dominant disorder that is usually caused by mutations in the MECP2 gene
  2. almost exclusively females
  3. infants appear to develop normally during first 6 to 18 months but then develop characteristic symptoms including:
    * slowed head & brain growth
    * loss of speech & motor skills
    * abnormal hand movements
    * sleep disturbances
    * breathing abnormalities
    * seizures

children with Rett Syndrom may also have autistic-like traits (e.g., deficits in social interactions) during early stages of the disorder

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14
Q

Chromosomal Abnormalities

Down Syndrome is a(n) ____ disorder. List the 3 types.

A

autosomal
1) Trisomy 21
2) Mosaic trisomy 21
3) Translocation trisomy 21

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15
Q

Chromosomal Abnormalities

The most common type of Down Syndrome is ____, which accounts for about ____% of all cases

A

trisomy 21; 95%

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16
Q

Chromosomal Abnormalities

The trisomy 21 type of Down Syndrome is due to the presence of what

A

an extra 21 chromosome in all cells of the body (each cell contains 47, instead of the usual 46 chromosomes)

17
Q

Chromosomal Abnormalities

Mosaic trisomy 21 accounts for ____% of all cases of Down Syndrome and occurs when?

A

1%; only some cells in the body contain an extra 21 chromosome

18
Q

Chromosomal Abnormalities

Translocation trisomy 21 accounts for ____% of all cases of Down Syndrome and is characterized by what?

A

4%; characterized by 46 chromosomes in all cells of the body with some cells having a full or partial chromosome 21 attached (translocated) to another chromosome (most often chromosome 14)

19
Q

Chromosomal Abnormalities

list the symptoms of Down Syndrome

A
  • intellectual disability (mild to moderate)
  • decreased muscle tone (hypotonia)
  • short stocky build
  • wide face
  • thick tongue
  • almond-shaped eyes
  • developmental delays
  • an elevated risk for vision & hearing problems
  • heart defects
  • hypothyroidism
  • Alzheimer’s
20
Q

Chromosomal Abnormalities

in terms of etiology, which 2 types of Down Syndrome are caused by an error during cell division

A

trisomy 21 & mosaic trisomy 21

21
Q

Chromosomal Abnormalities

what is the primary risk-factor of having a baby with trisomy 21

A

older maternal age (risk increases sharply after 30 years of age)

22
Q

Chromosomal Abnormalities

translocation trisomy 21 is due to what?

A

either an error in cell division or inherited from a parent carrier

23
Q

Genetic Disorders

Huntington’s Disease and Phenylketonuria (PKU) are ____ dominant disorders.

24
Q

Chromosomal Abnormalities

an autosomal dominant disorder means that these disorders are caused by what?

A

a single autosomal dominant gene

25
# **Chromosomal Abnormalities** 75%if 1 parent has Huntington's. disease, a biological child of that parent has ____% chance of inheriting the disease. When both parents have Huntington's, their biological child has a ____% chance of inheriting the disease.
50%; 75%
26
# **Chromosomal Abnormalities** what are **teratogens**
drugs, diseases, & environmental hazards that cause developmental defects in the embryo or fetus
27
# **Prenatal Development** exposure to teratogens during what timeframe after conception is likely to cause major structural damage
3 to 8 weeks after conception
28
# **Prenatal Development** difference(s) between *fetal alcohol syndrome (FAS)* and *partial fetal alcohol syndrome (pFAS)*
both have central nervous system dysfunction but with pFAS facial abnormalities are less severe and retarded physical growth may or not be present
29
# **Prenatal Development** exposure to alcohol during any stage of prenatal development can have harmful effects, but it's most likely to cause major defects when it occurs during this period when organs & structures are forming most rapidly
embryonic period (weeks 3 through 8)
30
# **Prenatal Development** prenatal exposure to cocaine during the first trimester can cause what?
spontaneous abortion
31
# **Prenatal Development** prenatal exposure can cause | aside from spontaneous abortion during 1st trimester
premature birth & low birth weight
32
# **Prenatal Development** characteristics of cocaine-exposed infants
irritability, overly reactive to environmental stimuli, shrill piercing cry, & difficulty calming & feeding
33
# **Prenatal Development** infants exposed to cocaine during pregnancy might experience these issues when school age. When adolescents?
**in school** motor, attention, memory, & behavior problems **in adolescence** difficulty with problem-solving & abstract reasoning & increased risk for delinquency
34
# **Prenatal Development** the consequences of prenatal exposure to cocaine are mediated by what factors
* the amount & potency of cocaine used by the pregnant mother * exposure to the following after birth: * poverty * insensitive caregiving * other risk factors assocaited with having a substance-abusing parent