Week 4 Structural Abnormalities & Birth Defects Flashcards

1
Q

any development of an organ or structure that is abnormal in form, structure, or position

A

congenital anomaly

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2
Q

any anomaly

A

malformation

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3
Q

underdevelopment of a tissue, organ, or the body

A

hypoplasia

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4
Q

complete failure of a tissue or an organ to develop

A

aplasia

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5
Q

the condition of having more than the normal number of fingers or toes; extra digit may be a boneless piece of soft tissue or fully formed

A

polydactylism

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6
Q

a congenital condition in which the proximal portions of the limbs are poorly developed or absent

A

phocomelia

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7
Q

the absence of one or more limbs

A

amelia

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8
Q

a structural abnormality that results in the failure of the fetus’ spine to close properly during the first month of gestation; accompanied by developmental insufficiencies of the brain, spinal cord, and/or meninges

A

spina bifida

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9
Q

condition where infants may be born with an open lesion on their spine along with damage to the nerves and spinal cord; this damage is usually permanent and usually results in paralysis of the legs

A

spina bifida

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10
Q

disorder in which most children exhibit mental disabilities, bowel and bladder complications, and/or hydrocephalus (excessive cerebrospinal fluid in the brain)

A

spina bifida

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11
Q

there is no cure for spina bifida, but treatments include surgery, medication, and physical therapy (T/F)

A

true

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12
Q

the most severe form of spina bifida characterized by the protrusion from an opening in the spine of both the malformed spinal cord and the meninges

A

myelomeningocele

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13
Q

form of spina bifida which occurs when the spinal cord develops normally but the meninges
protrude from a spinal opening

A

meningocele

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14
Q

the least severe form of spina bifida, in which one or more vertebrae are malformed
and covered by a layer of skin

A

occulta

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15
Q

underdevelopment or incomplete development of tissues due to decreased numbers of cells

A

hypoplasia

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16
Q

an absence of cells that leads to incomplete formation of limbs or organs; distal end of the bone may be missing or entire bone may be missing

A

aplasia

17
Q

occurs when the two sides of the palate fail to fuse during fetal development resulting in an opening between the palatine bones that form the roof of the mouth

A

cleft palate

18
Q

a separation of the two sides of the lip which may include the bones of the upper jaw (maxillae)

A

cleft lip

19
Q

majority of cases of cleft palate and cleft lip are due to genetic factors (T/F)

A

true

20
Q

cleft palate and cleft lip can only happen on one side or the other (T/F)

A

false

21
Q

condition in which individuals have difficulties identifying various colors and shades of colors

A

color blindness / color deficiency

22
Q

most of the time color blindness affects females (T/F)

A

false

23
Q

can distinguish between red and green when comparing the two but they can’t determine if a color is red or green when shown only one of the two colors

A

red/green color blindness

24
Q

cannot distinguish between blue and yellow, they see only white or gray (usually due to another disorder)

A

blue color blindness

25
Q

total colorblindness; very rare, hereditary, and usually associated with poor visual acuity and extreme sensitivity to light

A

achromatopsia

26
Q

a type of birthmark, also known as a strawberry mark, in which superficial blood vessels are enlarged

A

vascular nevus

27
Q

extra chromosome is present, usually
chromosome 21 or 22; linked to mother’s age; causes intellectual disability which varies in degree among other traits

A

Down syndrome (trisomy 21)

28
Q

the protrusion of an organ through the wall normally containing it, common in the groin and diaphragm

A

hernia