Hemochromatosis physical examination: Difference between revisions

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|Deposition of iron in basal ganglia
|Deposition of iron in basal ganglia
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| rowspan="2" |Endocrine
| rowspan="4" |Endocrine
|Pituitary gland
|Pituitary gland
|Menstrual abnormality
|Menstrual abnormality
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|Deposition of iron in Thyroid gland
|Deposition of iron in Thyroid gland
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|Pancreas
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|Polyuria polydipsia polyphagia
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|Polyuria polydipsia polyphagia
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|Deposition of iron in Pancreas
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|-
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|Adrenal gland
|
|Fatigue
|
|Polyuria Hypotension
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|Deposition of iron in Adrenal gland
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|-
|Dermatological
|Skin
|Cutaneous hyperpigmentation
|Sun exposed affeced mostly with tan of melanin grey
|iron damage skin, melanin hyperactivity responds thus color of melanin
|-
|Joints
| Metacarpophalangeal
Proximal interphalangeal
 
wrist
 
knee
|Pain
Stiffness
|Decreased ROM
Stiffness improve with rest
|Deposition of iron in articular cartilage
|-
|Cardiovascular
|Heart
Blood vessels
|Asymptomatic
Heart failure palpitation Hypertension
|Diastolic dysfunction
Arrhythmias
 
Dilated cardiomyopathy
|Deposition of iron in cardiac tissue and blood vessels
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| rowspan="2" |Gastrointestinal
|Liver
|Fatigue
Fatty diarrhea
 
Itching
 
Jaundice
 
Weight loss
|Hepatomegaly
Liver failure
 
Liver cancer
|Deposition of iron in liver
|-
|Gallbladder
|Right upper abdominal pain
|Tender hepatomegaly
|Multiple blood transfusion leading to hemochromatosis
|}
|}



Revision as of 16:42, 4 December 2017

Hemochromatosis Microchapters

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Overview

Historical Perspective

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Differentiating Hemochromatosis from other Diseases

Epidemiology and Demographics

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Diagnosis

Diagnostic Study of Choice

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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
Endocrine Pituitary gland Menstrual abnormality

Loss of libido

Loss of body hair

Amenorreha

Erictle ddysfuntion

Deposition of iron in Pituitary gland
Thyroid gland Fatigue Signs of hypothyroidsium Deposition of iron in Thyroid gland
Pancreas Polyuria polydipsia polyphagia Polyuria polydipsia polyphagia Deposition of iron in Pancreas
Adrenal gland Fatigue Polyuria Hypotension Deposition of iron in Adrenal gland
Dermatological Skin Cutaneous hyperpigmentation Sun exposed affeced mostly with tan of melanin grey iron damage skin, melanin hyperactivity responds thus color of melanin
Joints  Metacarpophalangeal

Proximal interphalangeal

wrist

knee

Pain

Stiffness

Decreased ROM

Stiffness improve with rest

Deposition of iron in articular cartilage
Cardiovascular Heart

Blood vessels

Asymptomatic

Heart failure palpitation Hypertension

Diastolic dysfunction

Arrhythmias

Dilated cardiomyopathy

Deposition of iron in cardiac tissue and blood vessels
Gastrointestinal Liver Fatigue

Fatty diarrhea

Itching

Jaundice

Weight loss

Hepatomegaly

Liver failure

Liver cancer

Deposition of iron in liver
Gallbladder Right upper abdominal pain Tender hepatomegaly Multiple blood transfusion leading to hemochromatosis

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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