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Dr. Ashay H. Nandeshwar
M. D., (Ayu)(Mumbai)
(Podar Govt. Medical College)
P.G.D.M.L.T., L.Lb. (Sch)
Lecturer V.P.A.M.C.
Sangli |
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But in SS: F type of Hemoglobin, the irregular shaped R.B.C agglutinate and forms clamp which casuses ischemia and leads to crisis.
Signs & Symptoms of S.C.D patients:
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In childhood they get rheumatoid arthritis like symptoms.
Sudden fall in Hemoglobin level.
Unbearable pain.
Involvement of multiple organs.
a) Heapatic failure.
b) Spleenic failure.
C) Renal failure.
Due to frequent haemolysis increased billirubin level because of which icterus is cammon in S.C.D patients
Bone crush is the chronic condition of S.C.D
Necrosis of the joints specially hip joint and shoulder joints. |
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What is sickle cell trait?
Sickle cell trait is a condition where the patient is Phenotypically normal and Genotypically abnormal.
The allele shows S:A type of Hemoglobin.
So though S.C.D is autosomal recessive disorder but I have seen in few casae the parents were normal but the children were showing S type of Hemoglobin. |
| Treatment: |
| In Allopathy there is no specific treatment, but when I started treatment with Ayurvedic medicines, we found the Morphological and Phenotypical changes in R.B.C and patient. The Blood Tranfusion and the crisis of the patients stopped. |
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