Did you know...
that you can add questions of your own to the question bank? Click here to try.

Malformations 07

Topic: Pathology

Created on Sunday, February 15 2009 by gliageek

Last modified on Sunday, February 15 2009.


Courtesy of Dr. Mark Cohen
The usual presentation of this malformation syndrome is?

 
        A) Severe psychomotor retardation, feeding difficulty, choreiform movements, myoclonic jerks
 
        B) Hydrocephalus, prominent occiput, poor head control
 
        C) Truncal ataxia, mental retardation
 
        D) Occipital encephalocele, polydactyly, polycystic kidneys, hepatic fibrosis
 
        E) Episodic hyperpnea, abnormal eye movements, ataxia, and mental retardation
 

 


Back to the question = Go back to the top of the page.
See another question like this one = Reload a different version of this question ().
Click here for a random question = Load a random question from the database.
Clone this question = Use this question as a template to create a totally NEW question.
Rate this question = Enter detailed rating for this question!
Average user rating for this question = 5 = How users like you have rated this question.
This question was created on February 15, 2009 by gliageek.
This question was last modified on February 15, 2009.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

ANSWERS AND EXPLANATIONS




A) Severe psychomotor retardation, feeding difficulty, choreiform movements, myoclonic jerks

This answer is incorrect.


Ponto(neo)cerebellar hypoplasia  (See References)

Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

 

 

 

 

 

 

 

 




B) Hydrocephalus, prominent occiput, poor head control

This answer is correct.


Typical early life presentation of Dandy-Walker syndrome  (See References)

Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

 

 

 

 

 

 

 

 




C) Truncal ataxia, mental retardation

This answer is incorrect.


Rhombencephalosynapsis is characterised by dorsal fusion of the cerebellar hemispheres, hypoplasia of the vermis, fusion of dentate nuclei and superior cerebellar peduncles  (See References)

Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

 

 

 

 

 

 

 

 




D) Occipital encephalocele, polydactyly, polycystic kidneys, hepatic fibrosis

This answer is incorrect.


Meckel-Gruber syndrome  (See References)

Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

 

 

 

 

 

 

 

 




E) Episodic hyperpnea, abnormal eye movements, ataxia, and mental retardation

This answer is incorrect.


Joubert syndrome, which shows much less dilatation of IVth ventricle, and many more abnormalities in roof nuclei  (See References)

Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

 

 

 

References:

1. Love, S., Louis, D.N., and Ellison, D.W. (2008). Greenfield's Neuropathology, 8th Edition. Oxford University Press, USA (ISBN:0340906820)Advertising:
2. Pasquier, L., Marcorelles, P., Loget, P., Pelluard, F., Carles, D., Perez, M., Bendavid, C., de La Rochebrochard, C., Ferry, M., David, V., Odent, S., and Laquerrière, A. (2009). "Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases." Acta Neuropathol, 117(2) 185-200. (PMID:19057916)
Back to the questionSee another question like this oneClick here for a random questionClone this question Rate this questionAverage user rating for this question = 5
Please log in if you want to rate questions.

 

FrontalCortex.com -- Neurology Review Questions -- Neurology Boards -- Board Review -- Residency Inservice Training Exam -- RITE Exam Review
pathology
Malformations 07
Question ID: 021509132
Question written by gliageek. (C) FrontalCortex.com 2006-2009, all rights reserved. Created: 02/15/2009
Modified: 02/15/2009
Estimated Permutations: 120
peer review status unavailable
rating unavailable


Top 5 tags for this item:
No tags have been created yet for this resource.
Please type in an appropriate tag for this item
more tags:
new tag:

User Comments About This Question:

0 user entries
Please log in if you'd like to add a comment.