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THE
CLINIC PROVIDES A FULL INVESTIGATIVE SERVICES : |
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The setup
has Forma Scientific, USA
:: CO2
incubator HERACELL® 150
:: SMZ1 Stereo Microscope with zoom lens
(Nikon, Japan)
:: A light microscope for semen evaluation.
:: OLYMPUS Inverted Microscope with Narishige
micromanipulator for ICSI
:: Laminar Flow hood (Klenzaids)
:: Oocyte recovery pump (craft UK)
:: Ultrasonography machine.
:: The centre has semen bank and Freezing
facilities whereby the husband can get his sperms stored and
not remain present for entire treatment.
:: Medison 9900 is a latest innovation with
color doppler, 3D & 4D facilities.
:: RI Saturn 3 Laser System |
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IUI
INTRAUTERINE INSEMINATION |
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Placement of sperms after
special treatment directly into the uterus. |
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IVF
IN-VITRO FERTILIZATION TEST TUBE BABY |
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Sperm
and eggs are collected, fertilized in the laboratory and
the resulting embryos replaced into the uterus. It is performed
in couples having blocked tubes, low sperm count, endometriosis,
unexplained infertility etc. Testicular biopsy.
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ICSI
(INTRA CYTOPLASMIC SPERM INJECTION) |
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The
centre has OLYMPUS Inverted Microscope with Narishige micromanipulator
for ICSI. ICSI is the injection of single sperm into each
vaible egg, the objective being to increase the chance of
fertilisation and development of embryo used in conjunction
with a IVF procedure. ICSI is designed to help couples where
male partner has recognised sperm problem, previously failed
IVF cycles, increased age of female partner etc. Retrieval
of sperms directly from the testes for use in ICSI.Assisted
hatching and Blastocyst Culture for improving success in
IVF and ICSI are also done here.
ICSI has had a great impact on male infertility as IVF had
on tubal infertility.
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CRYOPRESERVATION |
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Embryo freezing (Trivector) is used for Cryopreservation
of excess embryos which can be used in subsequent cycles.
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4-D
Ultrasound Scanner |
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You are about to experience a new
age of health care. A disease will be better understood,
detected and diagnosed at a much earlier stage.
Kaival Maternity Home and Surgical Hospital is now equipped
with revolutionary medical technology from Medison.
Medison 9900 is a latest innovation with color Doppler,3-D
and 4-D facilities.
Statistically about 4 to 5 congenital and maternal anomalies
are detected from every 100 pregnancies. Most common congenital
anomalies are cranio-spinal (head and spine) and cardiac
(heart) anomalies. They account for about 20-30 % perinatal
mortalities. These anomalies occur sporadically and can
not be anticipated. Imaging at right time enables us in
taking the right decision at the right time.
High resolution ultrasound with 3-D and 4-D facilities
enables us better visualization of normal and abnormal
foetal parts. We can find out many congenital anomalies
like abnormal development of brain, kidneys and limbs,
heart problems, any tumor in neck, chest or abdomen. Parents
can also appreciate the foetal parts like face, spine,
limbs, fingers and every single organ as if they are actually
looking at the foetus. 4-D ultrasound enables us to see
real time images of foetal movements like yawning, thumb
sucking, swallowing etc.
Along with this, we can have a photograph of your child
during intranterine (fetal) period and store it as a memory
in C.D / Photo.
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Consulting
Radiologist
Dr.Ritesh Prajapati
M.D,D.M.R.E. |
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RI SATURN
3 LASER SYSTEM |
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The world's
first directional laser for IVF. Utilising cutting edge
robotic technology |
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LASER ASSISTED HATCHING |
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A
covering layer, or 'shell' surrounds embryos or blastocysts
called the Zona Pellucida (ZP). The zona has an important
role in fertilisation as it allows only one sperm to penetrate
the zona and enter the egg to achieve fertilisation. It
also acts to prevent premature implantation in the Fallopian
tube and may help prevent the early embryo from being attacked
by cells of the immune system.
The embryos have to "hatch" or break out of the
zona in order to embed into the endometrium lining the uterine
cavity. This occurs about four to five days after embryo
transfer when the embryo is at the blastocyst stage. Naturally
this takes place by expanding/contracting of the zona until
it distorts, allowing the blastocyst to "hatch".
If the zona is not functional, this hatching may not occur.
It has been reported that up to 75% of normal embryos never
hatch through the protective layering of the zona. Laboratory
techniques involved in IVF may result in hardening of the
zona. In natural fertilsation there are enzymes present
within the fluid in the Fallopian tube, which may "soften"
the zona. This does not happen in IVF as the tube is bypassed.
The zona may also be thicker following IVF, especially in
older ladies. Frozen embryos may also have a hardened zona.
Who is suitable for Laser Assisted
Hatching?
At the London Fertility Centre patients who will be considered
for laser assisted hatching are:
:: Those patients who have IVF or
ICSI who are over 37 years
:: Patients having FER
:: Patients who have had a previous failed IVF or ICSI
treatment cycle
:: Patients undergoing IVF/ICSI for the first time, who
are considered poor responders because they have required
a high dose of gonadotrophins for poor ovarian response
:: Patients who in an earlier IVF cycle have had a low
fertilisation rate, for example, less than one third of
the embryos achieving fertilsation
:: Patients with three or fewer embryos
:: Patients who request laser assisted hatching and are
fully informed of its use and function
Embryo Freezing
Embryo freezing (called cryopreservation) is used in conjunction
with in vitro fertilization (IVF). Embryo freezing permits
high quality embryos that are not immediately used for
IVF to be frozen for the couple’s later use.
In a typical IVF cycle, the female partner undergoes
hormonal stimulation with fertility medication to ensure
that her ovaries produce enough eggs. In many cases, a
surplus of eggs are retrieved and successfully fertilized.
Selected embryos that are not immediately returned to
the woman’s uterus can be frozen in small vials
of liquid nitrogen and safely stored for decades.
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PGD |
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The Centre has the facility
for Pre Implantation genetic screening Chromosomes 18,
21 &22.
How is PGD Done?
Pre-implantation genetic diagnosis is used during an IVF
cycle to identify specific embryos that carry abnormal
genes. PGD is normally recommended for couples where one
or both of the parents are a known carrier of a genetic
disease (i.e. hemophilia or cystic fibrosis).
WHAT IS EMBRYO BIOPSY?
When an embryo reaches 4 to 8 cell stage (on day 2 or
day3) of development, one or two of these cells, called
“blastomeres,” can be removed from the embryo
with the same sort of micromanipulation technique that
is used for ICSI, and the embryo will be unharmed, and
can go on to develop just as though this one cell were
never removed. Every cell of the embryo at the four to
eight-cell stage is genetically identical to every other
cell, and any group of those cells will develop normally
on their own because they have the complete genetic potential
to develop into a normal embryo. You are not removing
any genetic material that is necessary for the complete
and normal expression of that embryo’s genes if
you take out a single cell at this stage. You can then
subject those one or two cells to genetic analysis, and
know thereby the genetic composition of the embryos. These
genetic tests can be performed within a day, giving plenty
of time to decide which embryos to transfer back to the
patient and which embryos not to transfer.
Who is Eligible for PGD?
When PGD was first offered to the public, it was meant
to be used only by those couples whose future children
were at "high risk" of developing a genetic
disorder. However, PGD was originally only offered at
a select few infertility clinics worldwide.
Who should be offered PGD:
Women over the age of 35 who have had miscarriages or
failed attempts at becoming pregnant through IVF
Women who have experienced recurrent miscarriages
Any couple who has repeatedly been unable to become pregnant
through multiple IVF cycles
Any couple where a man’s sperm count is low that
it is necessary to perform ICSI
What Genetic Diseases Can PGD Test For?
Numerous diseases and disorders classified as either chromosomal
disorders, single gene defects or sex-linked disorders
can be tested for through PGD. Specific chromosomes are
tested for specific disorders, including:
Chromosome 13: Breast and ovarian cancers, deafness, Wilson
Disease
Chromosome 15: Marfan Syndrome, Tay-Sach's Disease
Chromosome 16: Polycystic kidney disease, Alpha thalassemia
Chromosome 17: Charcot-Marie-Tooth Disease
Chromosome 18: Niemann-Pick Disease, pancreatic cancer
Chromosome 21: Down's Syndrome
Chromosome X: Duchenne muscular dystrophy, Turner's Syndrome,
Fragile X Syndrome
Chromosome Y: Acute myeloid leukemia
What are the risks?
Embryo biopsy procedures have been used extensively at
major IVF clinics throughout the world for PGD of both
single gene and chromosomal disorders. Follow up studies
have shown that the procedure is safe with no known adverse
affects on the embryo's potential to implant and develop
normally. Some studies have shown that biopsied embryos
may have a significantly better chance of implanting in
the uterus than non-biopsied embryos.
Due to the complexity of the genetic tests, it is possible
that a conclusive result is not obtained from all biopsied
embryos. In this case, the embryos will be left to grow
further and if they develop to blastocyst stage they will
be frozen.
Other PGD Facts
• Embryo biopsy does not appear to affect embryo
development.
• Only embryos that are good quality and adequately
developed can be biopsied.
• It may not be possible to obtain a result from
every embryo.
• It is not possible to test all chromosomes of
the embryo using PCR.
• The accuracy of the testing is high, but not 100%.
Prenatal testing is highly recommended in an ensuing pregnancy.
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ANDROLOGY |
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ENDOSCOPY CENTRE |
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HORMONE ASSAY |
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ALL FACILITIES UNDER
ONE ROOF |
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Embryo freezing (Trivector) is
used for Cryopreservation of excess embryos which can
be used in subsequent cycles.
The centre has also facilities for endoscopic surgeries,
sonography and endocrinological tests. The Akanksha infertility
centre can boast of innumerable IUI abd IVF pregnancies.
The team working in the centre are friendly, approachable
and highly knowledgeable and above all are geniunely committed
to helping couples achieve their goal and last but not
the least providing outstanding infertility treatment
at affordable price The Centre Has The facility for Pre
Implantation genetic screening Chromosomes 18, 21 &22.
"Unless you are prepared to keep your sight on tomorrow.
You cannot expect to be in touch with today.
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