Glands & Genetics Flashcards

1
Q

Explain how endocrine and exocrine glands are classified

A
  1. Glands are aggregations of cells which are designed to produce secretions (2 types: exocrine & endocrine)
  2. Exocrine glands secrete onto epithelial surface
  3. They develop from epithelia (epithelial calls invaginate into underlying connective tissue to form glands)
  4. 3 types of secretion mechanism: Merocrine = salivary gland; Apocrine = mammary gland; Holocrine = sebaceous gland
  5. Also classified based on secretion type: Serous = parotid salivary gland ; Mucous = sublingual; Mixed = submandibular
  6. Classified based on no. of cells: Single cell → goblet cells (fallopian tube)
    Multicellular → Duct = simple/compound
    → Secretory part = single/branched
    → Shape of secretory part = tubular/acinar
  7. Simple glands classified:
    → simple tubular = fundus of stomach, glands of colon
    → simple branched tubular = pylorus of stomach
    → simple coiled tubular = sweat glands
    → simple acinar = penile urethra
    → simple branched acinar = sebaceous glands
  8. Compound glands classified:
    → compound branched tubular = brunner’s glands
    → compound acinar = pancreas
    → compound tubuloacinar = prostate
  9. Endocrine gland characteristics include: dense blood supply, ductless, cells organized as cords
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2
Q

Monozygotic vs. Dizygotic twins

A
  1. Monozygotic:
    → Identical
    → Same sex
    → 1 ova fertilized by 1 sperm
  2. Dizygotic:
    → non-identical
    → different/same sex
    → 2 ova fertilized by 2 sperms
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3
Q

What are the different Extra embryonic tissue arrangements?

A
  1. Separation @ 2 cell stage: 2 placenta, 2 amniotic cavities, 2 chorionic cavities
  2. Separation @ early blastocyst stage: 1 placenta, 2 amniotic cavities, 1 chorionic cavity
  3. Separation @ bilaminar germ disc stage: 1 placenta, 1 amniotic cavity, 1 chorionic cavity

*Complications with separation of zygote:
1. Placental previa
2. Twin to twin transfusion syndrome
3. Conjoined twins

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4
Q

Basis of autosomal dominant disorders

A
  1. Mutation in any chromosome except sex chromosomes
  2. One dominant gene is enough to express the disorder
  3. Vertical inheritance can be seen
  4. Females + males are equally affected
  5. Homozygous recessive does not show the disorder
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5
Q

Sex chromosome anomalies

A
  1. Klinefelter syndrome (XXY)
    → long arms + legs, no facial hair, ↓testis
    → in males
  2. Turner’s syndrome (X)
    → short stature, low hairline, web neck
    → in females
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6
Q

Suspicious features at a neonatal exam

A
  1. Small head; low set ears & abnormally rotated
  2. Plagiocephaly
  3. Hyperteiorysm
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7
Q

Reasons for autosomal recessive

A
  1. Both sexes equally affected
  2. Presence of skipping generations
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8
Q

Reasons for X-linked dominant

A
  1. Affected females have 50% chance of transmitting disease to sons and daughters
  2. Affected males do not transmit to sons, but to all daughters
  3. More males affected than females
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9
Q

Importance of meiosis division

A
  1. Produces four cells with half number of chromosomes of parent cell
  2. ↑ genetic diversity, ↑ amount of variation within species
  3. Variations improve chance of species to adapt to environment + survive
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10
Q

The Cell Cycle

A
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11
Q

Fertilization

A
  1. Fusion of male and female pro nuclei to form zygote
  2. Penetration of corona radiata by sperm
  3. Penetration of zona pellucida by sperm
  4. Fusion of pro nuclei
  5. Results in commencement of mitotic division
  6. Is possible to be performed in-vitro
  7. Ampullary region of fallopian tube is the most common site of fertilization
  8. POST wall of upper uterine segment is the site of implantation
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12
Q

Cells & Organelles

A
  1. Nucleus communicates with cytoplasm through nuclear pores
  2. Nuclei are not present in dormant nuclei
  3. Ribosomes are found within mitochondria, endoplasmic reticulum & cytoplasm
  4. Nuclei in active cells are large and small in inactive cells
  5. Nuclei in active cells have more euchromatin
  6. Mitochondria are inherited from mother (contain DNA)
  7. Glycocalyx is important in cell adhesion
  8. Nucleolus has both DNA & RNA
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13
Q

Polymorphic genes

A
  1. Causes variations in monogenic traits
  2. Does not maintain key features of species.
  3. Its frequency in a population determines the survival of the allele
  4. has a particular/fixed locus in a genome of a given species
  5. Phenotype is affected by environmental factors
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14
Q

Nervous system

A
  1. White matter indicates nerve fibers
  2. Grey matter indicates nerve cell bodies.
  3. Dermatome is supplied by a single spinal nerve root.
  4. Sympathetic ganglia found close to spinal cord (parasympathetic are close to the organ)
  5. PNS → satellite cells & Schwann cells
  6. CNS → astrocytes, oligodendrocytes, ependymal cells, microglial cells
  7. Somatic sensory nerve fibers carry sensations from muscle, skin, tendon, joints
  8. PS system has shorter postganglionic fibers than sympathetic system
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15
Q

Polygenic traits

A
  1. Are determined by allele on different loci
  2. Are qualitative traits
  3. Modified by environmental factors
  4. Contribute to variations in a population
  5. House keeping genes are responsible for stabilizing key features of species
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16
Q

Spermatogenesis

A
  1. Occurs in seminiferous tubules
  2. Spermatogonia undergo mitosis
  3. Begins after puberty
  4. Each primary spermatocyte gives rise to 4 haploid spermatids
  5. Sertoli cells support the process
17
Q

Ovum

A
  1. When ovulated it is called secondary oocyte
  2. Second meiotic division is completed after fertilization
  3. Is covered with Zona Pellucida
  4. Is influenced by LH
  5. Directly released into peritoneal cavity
18
Q

Sites of glands

A
  1. Simple tubular → intestinal crypts (LI = goblet cells; SI = columnar cells)
  2. Simple coiled tubular → sweat glands
  3. Simple branched tubular → gastric glands
  4. Simple acinar → penile urethra
  5. Simple branched acinar → sebaceous glands
  6. Compound branched tubular → duodenum
  7. Compound acinar → pancreas, mammary gland, parotid gland
  8. Compound tubulo-acinar → submandibular gland