Hemochromatosis physical examination: Difference between revisions

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* [[Erectile dysfunction]] and [[hypogonadism]]
* [[Erectile dysfunction]] and [[hypogonadism]]
* Congestive [[heart failure]], [[arrhythmia]]s or [[pericarditis]]
* Congestive [[heart failure]], [[arrhythmia]]s or [[pericarditis]]
* [[Deafness]]<ref name=Jones_1983>{{cite journal |author=Jones H, Hedley-Whyte E |title=Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs |journal=Neurology |volume=33 |issue=11 |pages=1479-83 |year=1983 |pmid=6685241}}</ref>
* [[Deafness]]<ref name="Jones_1983">{{cite journal |author=Jones H, Hedley-Whyte E |title=Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs |journal=Neurology |volume=33 |issue=11 |pages=1479-83 |year=1983 |pmid=6685241}}</ref>
*[[Dyskinesia]]s, including [[Parkinsonian]] symptoms<ref name=Costello_2004>{{cite journal |author=Costello D, Walsh S, Harrington H, Walsh C |title=Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series |journal=J Neurol Neurosurg Psychiatry |volume=75 |issue=4 |pages=631-3 |year=2004 |pmid=15026513}}</ref><ref name=Jones_1983 /><ref name=Nielsen_1995>{{cite journal |author=Nielsen J, Jensen L, Krabbe K |title=Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome |journal=J Neurol Neurosurg Psychiatry |volume=59 |issue=3 |pages=318-21 |year=1995 |pmid=7673967}}</ref>
*[[Dyskinesia]]s, including [[Parkinsonian]] symptoms<ref name="Costello_2004">{{cite journal |author=Costello D, Walsh S, Harrington H, Walsh C |title=Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series |journal=J Neurol Neurosurg Psychiatry |volume=75 |issue=4 |pages=631-3 |year=2004 |pmid=15026513}}</ref><ref name="Jones_1983" /><ref name="Nielsen_1995">{{cite journal |author=Nielsen J, Jensen L, Krabbe K |title=Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome |journal=J Neurol Neurosurg Psychiatry |volume=59 |issue=3 |pages=318-21 |year=1995 |pmid=7673967}}</ref>
* Dysfunction of certain [[endocrine organs]]:
* Dysfunction of certain [[endocrine organs]]:
** [[Pancreas|Pancreatic gland]], as above, manifesting as [[diabetes]]
** [[Pancreas|Pancreatic gland]], as above, manifesting as [[diabetes]]
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Males are usually diagnosed after their forties, and women about a decade later, owing to regular iron loss by [[menstruation]] (which ceases in [[menopause]]).  Cases of [[iron]] overload have been found in young children as well.
Males are usually diagnosed after their forties, and women about a decade later, owing to regular iron loss by [[menstruation]] (which ceases in [[menopause]]).  Cases of [[iron]] overload have been found in young children as well.
{| class="wikitable"
!System involved
!Organs
!Symptom
!Signs
!Mechanisum
!
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| rowspan="2" |Nervous system
|PNS
|Parastheisa
Loss of motor control
|Loss of two point discrimination
Hyporeflaxia decreased power
|Axonal sensory motor polyneuropathy
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|CNS
|Abnormal gait
Dementia
|Dyskinesias(parkinsonian syndrome Multiple sclerosis)
cognitive decline
|Deposition of iron in basal ganglia
|
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==References==
==References==

Revision as of 16:05, 4 December 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Physical Examination

Males are usually diagnosed after their forties, and women about a decade later, owing to regular iron loss by menstruation (which ceases in menopause). Cases of iron overload have been found in young children as well.

System involved Organs Symptom Signs Mechanisum
Nervous system PNS Parastheisa

Loss of motor control

Loss of two point discrimination

Hyporeflaxia decreased power

Axonal sensory motor polyneuropathy
CNS Abnormal gait

Dementia

Dyskinesias(parkinsonian syndrome Multiple sclerosis)

cognitive decline

Deposition of iron in basal ganglia

References

  1. 1.0 1.1 Jones H, Hedley-Whyte E (1983). "Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs". Neurology. 33 (11): 1479–83. PMID 6685241.
  2. Costello D, Walsh S, Harrington H, Walsh C (2004). "Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series". J Neurol Neurosurg Psychiatry. 75 (4): 631–3. PMID 15026513.
  3. Nielsen J, Jensen L, Krabbe K (1995). "Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome". J Neurol Neurosurg Psychiatry. 59 (3): 318–21. PMID 7673967.

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