Embryo 1 Flashcards

1
Q

Complete Hydatiform Mole

A

EITHER:

1) Fertilization of an empty oocyte, followed by sperm duplication
2) Fertilization of an empty oocyte by 2 sperm

Formed in the first week

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2
Q

Partial Hydatiform Mole

A

Fertilization of a normal oocyte by 2 sperm

Formed in the first week

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3
Q

Symptoms of the Hydratidiform Moles

A

Vaginal bleeding
Pelvic pressure and/or pain
Enlarged uterus
Hyperemesis Gravidarum (morning sickness)

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4
Q

Choriocarcinomas

A

Malignant tumors which develop from the hydratidiform moles
Can spread to lungs, bone, vagina, and brain
Post week 1 issue

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5
Q

Abnormal Implantation

A

Ectopic pregnancy- occurs outside the uterus, like the abdominal
They are most commonly found in the proximal uterine tube

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6
Q

Placenta Previa

A

Implantation occurs in the internal cervical os, which blocks it
Beyond 20 weeks of gestation, there is vaginal bleeding
1) Marginal placenta previa
2) Partial placenta previa
3) Total Placenta previa
Do a sonogram before doing a digital exam so you don’t cause hemorrhage

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7
Q

Chordomas

A

Rare slow growing aggressive neoplasms of bone
* Arise from the remenants of the notochord
Occur in the axial skeleton of the spheo-occipital region of skull and sacral regions
Week 3 issue

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8
Q

Sacrococcygeal Teratoma

A

Tumor in the tailbone of the baby, due to the primative streak persisting and not going away
All three germ layers can be found in them
Week 3 issue

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9
Q

Oropharyngeal Teratoma

A

Tumors in the mouth that are due to the persistance of the primative streak
Week 3 issue

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10
Q

Hirschsprungs Disease

A

Neurocristopathy in which the autonomic system doesn’t innervate the colon, so you can’t poop

Defect in the migration or morphogensis in the trunk neural crest **extra info

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11
Q

Albinism

A

Neural crest defect with the damn pigment cells that arise from neural crest

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12
Q

DiGeorge Syndrome

A

Hypothyroidism, thyroid deficiency, thymic displasia leading to immunodeficiency, defects in cardiac flow and the aortic arches

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13
Q

Dental anomalies

A

Since neural crest cells deal with enamel and dentin, issues arise from that

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14
Q

Neuroblastoma

A

Tumor of adrenal medulla and/or autonomic ganglia

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15
Q

Spinal bifida Occulta

A

Neural tube defect of the caudal pore
There is an unfused verterbral arch, due to the the failure of the caudal neural pore to close at the appropriate time
Nothing wrong with the person except that they have a tuft of hair on the end of their spine

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16
Q

Meningoecele

A

Meninge-cist, doesn’t close on time but eventually closed
No vertebral or neuro arches
The pouches are filled with cerebral spinal fluid
Patients may or may not see abnormalities
Neural tube defect in caudal pore

17
Q

Meningomyelocele

A

Neural tube protrudes out in the cist and filled with cerbral final fluid
Experience motor and sensory deficit
Neural tube defect on the caudal neural

18
Q

Myelocele

A

The spinal chord is open must be surgically corrected and there is a motor and sensory deficit
Caudal Neural pore issue of the neuro tube

19
Q

Anencephaly

A

Problem with close of rostral neuropore
Not compatible with life
No brain cap

20
Q

Enencephalocele

A

Big lump on the back of your head
Rostral neuro pore closing
Not compatible with life
Can be an issue with or without brain tissue

21
Q

Occipital Mylocoele

A

Failure in rostral closing and you get a lump in the occipital region

22
Q

Frontal Encephylocoele

A

Failure in rostral neural pore closing

The issue happens by day 28

23
Q

Thoracic outlet syndrome

A

Cervical ribs can compress arteries and can lead to blockage

24
Q

Pectus Carinatum

A

Sternum protrudes leading to pigeon chest

No real issues, just looks weird

25
Q

Pectus Excavatum

A

Sternum is depressed creating a “funnel chest”
This can compress or move the heart and can decrease the amount of air someone gets
Can be surgically corrected

26
Q

Poland syndrome

A

Associated with syndactyly-> fused digits
Absence of pectoralis major and minor
Ipsilateral breast hypoplasia- the pec isn’t well developed
Absence of 2 to 4 ribs
**Due to the absence of migration of the hypomere into the chest, which causes the absence of the pectoralis major

27
Q

Prune-Belly Syndrome

A

Partial or complete absence of abdominal musculature due to the absence or abnormal migration of the hypomere cells
Primarily affects males
Associated with: 1) Cyptorchidism- one or both testes won’t descend
2) Malformation of urinary tract and bladder leading to urethral obstruction

28
Q

Talipes Equinovarus- AKA Clubbed Foot

A

• Most common musculoskeletal
defect
• Sole of foot turned medially and foot is inverted
• 2x more frequent in males
• All anatomical structures present so cases can be treated with casting or taping
Due to the insufficient amount of amniotic fluid

29
Q

Developmental Hip Dysplasia

A

More common in females than males
• Under development of the acetabulum of the hip bone
-So you get a disclocation of the hip bone
• Generalized joint laxity

30
Q

Arthrogryposis (congenital joint contractures)

A
• Usually involves more than 1 joint
• Causes: unclear, but thought to be due to:
– Neurological defects
– Muscularabnormalities
– Joint and contiguous tissue problems
– Fetalcrowding
31
Q

Meromelia

A
  • Absence of part of a limb

* Intermediate to late loss of FGF signaling

32
Q

Amelia

A

Loss of a whole limb

Loss of FGF signaling

33
Q

Phocomelia

A

Loss of long bones
Hands or feet are attached to body
Partial loss of FGF signaling or HOX disruption
Thalomide

34
Q

Ectrodacytyly

A

Split hand or foot
Lobster claw deformity
Partial absence of FGF 8 from AER

35
Q

Polydactyly

A

Extra digits
Overexpression of SHH and upregulation or duplication of ZPA
Duplication would result in two sets
Week 6 or week 7 issue depending on the affected limb
Hand- Week 6
Foot- Week 7

36
Q

Syndactyly

A

Fusion of bones (osseous) or webbing between digits (cutaneous)
Digital rays fail to develop and apoptosis between them didn’t happen
BMP disruption or HOXD13 mutation