Chapter 29: Development and Inheritance Flashcards

1
Q

Eclampsia

A

A condition in which one or more convulsions occur in a pregnant woman suffering from high blood pressure, often followed by coma and posing a threat to the health of mother and baby.

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2
Q

Gamete Intrafallopian Transfer (GIFT)

A

An assisted reproductive procedure in which a woman’s eggs are removed, mixed with sperm, and replaced into the woman’s uterine tube where the fertilization takes place, rather than in the laboratory.

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3
Q

In Vitro Fertilization

A

Fertilization outside the body, generally in a Petri dish.

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4
Q

Infertility

A

The inability to achieve pregnancy after engaging in 1 year of appropriately timed intercourse.

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5
Q

Neural Tube Defects (NTDs)

A

Major birth defects caused by an abnormal development of the neural tube—the structure present during the embryonic stage that later becomes the CNS. These are very common birth defects that cause infant mortality and disability and include anencephaly and spina bifida.

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6
Q

Placenta Abruptio

A

Condition in which there is separation of the placenta from the uterine site of implantation before delivery of the baby.

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7
Q

Placenta Previa

A

Condition during pregnancy in which the placenta is abnormally placed so as to totally or partially cover the cervix.

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8
Q

Pre-eclampsia

A

Condition during pregnancy characterized by sudden HTN, albuminuria, and edema of the hands, feet, and face. It is the most common complication of pregnancy, affecting about 5% of pregnancies.

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9
Q

Therapeutic Cloning

A

A procedure that usually takes skin cells form a patient, and inserts a skin cell nucleus into the fertilized egg whose nucleus has been removed to create a new cell. That new cell divides repeatedly to form a blastocyst from which stem cells can be extracted to grow new tissue that is genetically matched to the patient.

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10
Q

Abortion

A

The premature loss or expulsion of an embryo or fetus.

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11
Q

Amnion

A

One of the four extra-embryonic membranes; surrounds the developing embryo or fetus.

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12
Q

Amniotic Fluid

A

Fluid that fills the amnitotic cavity; cushions and supports the embryo or fetus.

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13
Q

Autosomes

A

A chromosomes other than the X or Y sex chromosomes.

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14
Q

Chorion

A

An extra-embryonic membrane, consisting of the trophoblast and underlying mesoderm, that forms the placenta.

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15
Q

Chromosomes

A

Dense structures, composed of tightly coiled DNA strands and associated histones, that become visible in the nucleus when a cell prepares to undergo mitosis or meiosis; normal human somatic cells each contain 46 chromosomes.

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16
Q

Differentiation

A

The gradual appearance of characteristic cellular specializations during development as the result of gene activation or repression.

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17
Q

Down Syndrome

A

A genetic abnormality resulting from the presence of three copies of chromosome 21; people with this condition have characteristic physical and intellectual deficits; also called Trisomy.

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18
Q

Ectoderm

A

One of the three primary germ layers; covers the surface of the embryo and gives rise to the nervous system, the epidermis and associated glands, and a variety of other structures.

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19
Q

Ectopic Pregnancy

A

Outside the normal location, pregnancy.

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20
Q

Embryo

A

The development stage beginning at fertilization and ending at the start of the third development.

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21
Q

Embryology

A

The study of embryonic development, focusing on the first 2 months after fertilization.

22
Q

Endoderm

A

One of the three primary germ layers; the layer on the undersurface of the embryonic disc; gives rise to the epithelia and glands of the digestive system, the respiratory system, and portions of the urinary system.

23
Q

Extra-embryonic Membranes

A

The yolk sac, amnion, chorion, and allantois.

24
Q

Fetus

A

The development stage lasting from the start of the third development month to delivery.

25
Q

Genes

A

A portion of a DNA strand that functions as a hereditary unit, is located at a particular site on a specific chromosome, and codes for a specific protein or polypeptide.

26
Q

Genetics

A

The study of heredity and genetic variations.

27
Q

Genotype

A

Genetic makeup of an organism.

28
Q

Heterozygous

A

Possessing two different alleles at corresponding sites on a chromosome pair; a person’s phenotype is determined by one or both of the alleles.

29
Q

Human Chorionic Gonadotropin (hCG)

A

The placental hormone that maintains the corpus luteum for the first three months of pregnancy.

30
Q

Human Placental Lactogen (hPL)

A

The placental hormone that stimulates that functional development of the mammary glands.

31
Q

Hyaluronidase

A

An enzyme that breaks down the bonds between adjacent follicle cells; produced by some bacteria and found in the acrosome of a sperm.

32
Q

Implantation

A

The attachment of a blastocyte into the endometrium of the uterine wall.

33
Q

Inner Cell Mass

A

Cells of the blastocyst that will form the body of the embryo.

34
Q

Lacunae

A

A small pit or cavity.

35
Q

Mesoderm

A

The middle germ layer, between the ectoderm and endoderm of the embryo.

36
Q

Neonate

A

A newborn infant, or baby.

37
Q

Oocyte

A

A cell whose meiotic divisions will produce a single ovum and three polar bodies.

38
Q

Organogenesis

A

The formation of organs during embryonic and fetal development.

39
Q

Ovum

A

The functional product of meiosis II, produced after the fertilization of a secondary oocyte.

40
Q

Phenotype

A

Physical characteristics that are genetically determined.

41
Q

Placenta

A

A temporary structure in the uterine wall that permits diffusion between the fetal and maternal circulatory systems.

42
Q

Puberty

A

A period of rapid growth, sexual maturation, and the appearance of secondary sexual characteristics; normally occurs at ages 10-15 yrs.

43
Q

Relaxin

A

A hormone that loosens the pubic symphysis; secreted by the placenta.

44
Q

Senescence

A

Aging.

45
Q

Sperm

A

Male gamete(s).

46
Q

Trisomy

A

see Down Syndrome: The abnormal possession of three copies of a chromosome; trisomy 21 is responsible for Down Syndrome.

47
Q

Umbilical Cord

A

The connecting stalk between the fetus and the placenta; contains the allantois, the umbilical arteries, and the umbilical vein.

48
Q

Villi

A

Slender, finger-shaped projection(s) of a mucous membrane.

49
Q

X Chromosomes

A

One of two sex chromosomes; females have two X chromosomes.

50
Q

Y Chromosomes

A

The sex chromosomes whose presence indicates that the individual is a genetic male.