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EngineerinG
Inventor’s
mouth.
Consequences of my research.
Introduction.
Mysteries in
genetic sciences.
What is
coronary artery disease?
Misconceptions in cardio-vascular
sciences.
Foundation
on which building of Baruah Applied Human.
Revolution in medical sciences rocked by
Dr.D.R. Baruah,FRCSGlas.
Unfolding the
mysteries in human genetic sciences.
Mysteries in
human genetic sciences.
How does the
mutation expresses in particular disease form?
Selection of
patients for gene analysis
Eradication of
heart disease & rarest of the rare diseases- Human genetic studies
through sequencing of m-RNA.
Signal
Transduction plays a major role during pre-bypass and post-bypass
events.
How bypass
surgery triggers signal transduction & phenotypically expressed.
Mutation
Selection of
genes causing heart & other diseases.
Hypoxia,
reactive oxygen species, intracellular calcium & Baruah syndrome.
Re-sequencing
of the following genes to identify the mysteries.
First time on
this planet– Genovac.
Baruah applied
human genetic engineering- a choice of treatment for Cancer.
TGA-A New
Method of Treatment of Complex Congenital Heart Disease.
Endocardial Cushion defect.
Genetic
Engineering–To cure the rarest of the rare autoimmune.
First time on
the Planet–Manifestation of Baruah Syndrome–Moyamoya
The rarest of
the rare genetic disorder–Takayasu.
Isolated
congenital Right Ventricular Hypertrophy.
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Applied Human Genetic Engineering - Vol.II |
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TGA-A New Method of Treatment of Complex Congenital Heart Disease-A
Revolution in Medical
SciencE
 Abstract
:-
A
complex
congenital heart disease such as transposition of great
arteries (TGA) with or without ASD
or VSD is not known to be
uncommon. The child is borne with TGA with or without
ASD or VSD, the common cause of blue babies is
known to all clinicians. The child borne with TGA
without ASD or VSD and without having patency of ductus aortus
has incidence of survival of more than few hours, which
is very remote. Atrial septostomy was a standard
procedure for long run survival.
Infusion of prostaglandin is used to keep the PDA
patency as a short term therapy, is also a standard
medical practice before taking the patient for
corrective surgical procedure. Mustard procedure was a
standard one at atrial level which was changed to
Senning procedure in different stages of childhood.
Switch surgical procedure had started some years ago and
it is now a standard surgical procedure of TGA and this
should be done within 72 hours after child is borne to
obtain good results. However, late
complications like stenosis of pulmonary artery and
aorta were reported. (TGA-Shilpajyoti
Kashyap treated at the age of 9 with Baruah Biological
molecules. Her shunt was reversed with asymptomatic with
Baruah applied human genetic engineering treatment since
2002.)
We have used a newly
developed isolated plant organic compounds for an eleven
year old baby with TGA & VSD where signs and symptoms
disappeared and child’s condition has improved
clinically and behaving like a normal child. With this
discovery, the new era of treatment of congenital
anomalies with drugs isolated from medicinal plants has
started, which is presented here.
 Introduction:-
Cyanosis
of lips, finger nails, toes, breathlessness, chronic
chest infection with cough and cold and fever,
retardation of mental and physical growth, low exercise
tolerance are the common features of TGA with VSD in
later days of childhood. This group of patients do not
usually survive beyond their teenage as reported. At
this stage, heart-lung transplant has become a standard
surgical procedure
 History:-
Eleven year old girl
was brought by parents with following congenital anomaly
to our clinic in month of July 2003. She attended two
another hospitals where she was sent back home saying
that there is no surgical or medical treatment available
at this stage. The child had the following signs,
symptoms and diagnosis.
Ventricular septal defect (VSD)
TGA
Severe PAH- right to left shunt
Congestion of both liver with impaired liver
function
Loss of appetite
Frequent motions and unable to digest the food
Stunted growth
Unable to concentrate her studies
Exercise tolerance was poor and unable to play like
a normal child.
Nail beds and lips were completely blue
Clubbing of toes and fingers present
Breathlessness on
minimal exertion
Hemoglobin was 18mg%
Colour echocardiography studies reveals VSD, severe
PAH- VSD-8mm in size with right to left shunt
Her parents were
agreed to go for heart-lung transplant using pig as a
donor. However, as a first step, we have treated her
with Baruah biological molecules and treatment was
started from July 5 th,
2003.
Results:-
Three days later, her
chest infection and congestion began to disappear and
breathlessness was reduced . Blueness of lips, toes and
finger nails began to disappear and became pink. Six days later, she
regained her appetite and food intake was increased. We
continued the same treatment and on 29th
July, post-treatment echo with colour Doppler
echocardiography was done.
The following findings
were observed:-
VSD was measured to be
8mm in size and right to left shunt was changed to left
to right with normal ventricular function.
No pulmonary
hypertension, which was reported earlier.
Hemoglobin was reduced
by 3mg%
She could climb up the
hill, she could ride bicycle without exertion. Chest infection was
disappeared. Heart size reduced by 1cm. Lung fields were
clear. She puts on weight by 2.5 Kgs in 60 days. Clubbing of toes and
finger nails were completely disappeared. Hemoglobin was
reduced further to 12mg%. Echocardiography
studies with colour Doppler in 60 days therapy, reveals
that there is no PAH. VSD remains with same diameter.
Left to right shunt continues. She has gone back to her
school with unrestricted activities. She is continuing
the treatment with plant organic compounds and she is
surviving without heart-lung transplant.
 Discussion:
Our organic compounds from medicinal
plants have reduced the higher pressure of morphological
right ventricle which is functional left ventricle
allowing shunt to reverse where ratio of deoxygenated
and oxygenated blood was changed resulting disappearance
of cyanosis, improvement of liver function and exercise
tolerance. Patients with complex congenital heart
disease such as TGA with VSD do not have incidence of
long term survival. They have a continuous problems like
chest infection, mental retardation, stunted growth, not
doing well in the school, breathlessness, and not
gaining weight. Heart –lung transplant is the only
surgical procedure can be undertaken for these patients
with low incidence of survival. High Pulmonary pressure
is the major problem. Reduction of PA pressure with
reversal of shunt are not known till today treated with
conventional therapy such as diuretics, digitalis. This
is probably for the first time treated successfully with
isolated plant organic compounds. However, long-term
results are yet to be seen with this therapy.
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