USMLE STEP 1 NEUROLOGY Questions and Answers with Complete Solutions 2024
33 views 0 purchase
Course
USMLE STEP 1
Institution
USMLE STEP 1
USMLE STEP 1 NEUROLOGY Questions
and Answers with Complete Solutions 2024
The notochord induces what to differentiate into what? - ANSInduces
overlying ECTODERM to differentiate into NEUROECTODERM and form
NUERAL PLATE
Neural plate then gives rise to? - ANSNeural tube and neural crest cells
N...
USMLE STEP 1 NEURO LOGY Questions and Answers with Complete Solutions 2024 The notochord induces what to differentiate into what? - ANS✓✓Induces overlying ECTODERM to differentiate into NEUROECTODERM and form NUERAL PLATE Neural plate then gives rise to? - ANS✓✓Neural tube and neural crest cells Notochord becomes what? - ANS✓✓Nucleus pulposus of the intervertebral disks in adults Alar Plate - ANS✓✓Dorsal [Sensory] Same orientation as spinal cord Basal Plate - ANS✓✓Ventral [Motor] Same orientation as the spinal cord How does FGF affect chordin and noggin? - ANS✓✓FGF regulates chordin and noggin to down regulate BMP which leads to neural plate induction Three Primary Vesicles - ANS✓✓1. Forebrain [Prosencephalon] 2. Midbrain [Mesencephalon] 3. Hindbrain [Rhombencphaln] The Forebrain gives rise to: - ANS✓✓1. Telencephalon [Cerebral hemispheres, lateral ventricles] 2. Diencephalon [Thalamus, Third Ventricle] The Midbrain gives rise to: - ANS✓✓1. Mesencephalon [Midbrain, aqueduct] The Hindbrain gives rise to: - ANS✓✓1. Metencephalon [Pons, cerebellum, upper part of the fourth ventricle] 2. Myelencephalon [Medulla, Lower part of the fourth ventricle] CNS/PNS Origins - ANS✓✓Neuroectoderm = CNS neurons, ependymal cell [Inner lining of ventricles, makes CSF], oligodendrocytes, astrocytes Neural crest cells = PNS, schwann cells Mesoderm = Microglia [Like Macrophages, originate from Mesoderm] Neural tube defects - ANS✓✓NEUROPORES fail to fuse [4th week] → Persistent connection between amniotic cavity and spinal canal Associated with: 1. Low folate levels before conception and during pregnancy 2. ↑ a -fetoprotein levels [AFP] in amniotic and maternal serum 3. ↑ AChE in amniotic fluid [Helpful confirmatory test] -- Fetal AChe in CSF transudates across defect into amniotic fluid Spina bifida occulta - ANS✓✓Failure of bony spinal canal to close, NO STRUCTURAL HERNIATION Usually seen at lower vertebral levels DURA INTACT Associated w/ tuft of hair or skin dimple at level of bony defect NORMAL AFP Meningocele - ANS✓✓Meninges [BUT NO NEURAL TISSUES] herniates through bony defect Meningomyelocele - ANS✓✓Meninges and neural tissue herniate through bony defect Associated w/ Arnold -Chiari Type II Malformation Anencephaly - ANS✓✓Malformation of the ANTERIOR NEURAL TUBE → 1. No forebrain 2. Open calvarium Clinical Findings: 1. ↑ a -fetoprotein levels [AFP] 2. Polyhydramnios [No swallowing center in brain] 3. Associated w/ MATERNAL TYPE I DIABETES 4. Maternal folate supplementation ↓ risk Holoprosencephaly - ANS✓✓Failure of LEFT AND RIGHT HEMISPHERES TO SEPARATE Usually occurs during the 5th and 6th week May be related to mutations in the SONIC HEDGEHOG signaling pathway Moderate form = Cleft lip/palate Severe form = Cyclopia Seen in: 1. PATAU SYNDROME 2. FETAL ALCOHOL SYNDROME Chiari Type II Malformation - ANS✓✓Posterior fossa malformation Significant HERNIATION of the CEREBELLAR TONSILS and VERMIS through FORAMEN MAGNUM with AQUEDUCTAL STENOSIS and HYDROCEPHALUS Patients often present w/: 1. Lumbosacral meningomyelocele 2. Paralysis below the defect Dandy -Walker Malformation - ANS✓✓AGENESIS of CEREBELLAR VERMIS with CYSTIC ENLARGEMENT of the 4th ventricle Fills enlarged posterior fossa Associated w/: 1. Hydrocephalus 2. Spina bifida Syringomyelia - ANS✓✓Cystic cavity [Syrinx] within SPINAL CORD If central canal = Hydromyelia Crossing anterior spinal commissural fibers are typically damaged CAPE -LIKE BILATERAL LOSS OF PAIN and TEMPERATURE in the UPPER EXTREMITIES Fine touch sensation is preserved Associated w/: 1. Arnold Chiari malformation 2. Trauma 3. Tumor Most common C8 -T1 [CERVICAL ENLARGEMENT] Arnold Chiari Type I Malformation - ANS✓✓CEREBELLAR TONSILLAR ECTOPIA > 3 -5 mm Congenital Usually asymptomatic in childhood Manifests w/ HEADACHE and CEREBELLAR SYMPTOMS Which arches form the anterior 2/3rds of the tongue - ANS✓✓1st and 2nd brachial arches -- Sensation via CN V -- Taste via CN VII Which arches form the posterior 1/3rd of the tongue - ANS✓✓3rd and 4th brachial arches --Sensation and taste via CN IX -- Extreme posterior vagus Motor innervation of the tongue - ANS✓✓CN XII [Hypoglossal nerve] to: 1. Hyoglossus = Retracts and depresses tongue
The benefits of buying summaries with Stuvia:
Guaranteed quality through customer reviews
Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.
Quick and easy check-out
You can quickly pay through EFT, credit card or Stuvia-credit for the summaries. There is no membership needed.
Focus on what matters
Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!
Frequently asked questions
What do I get when I buy this document?
You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.
Satisfaction guarantee: how does it work?
Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.
Who am I buying this summary from?
Stuvia is a marketplace, so you are not buying this document from us, but from seller Brainbarter. Stuvia facilitates payment to the seller.
Will I be stuck with a subscription?
No, you only buy this summary for R232,97. You're not tied to anything after your purchase.