New all in one universal blood test screening for the most common inherited genetic disorders
this is my: Gene 100+ UK Launch coming soon
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Diseases Are Preventable
Each year millions of healthy parents are taken by surprise when their children are born with life-threatening genetic disorders. These parents are carriers: healthy individuals who nevertheless have a mutant version of a critical gene. More than 2400 children are born with cystic fibrosis each year in the uk. The uk afro-Caribbean population are at risk of sickle-cell disease and the uk asain population are at risk of thalassemia. The UK Jewish community is affected by a vastly disproportionate share of genetic diseases. We can now end this needless suffering with a single inexpensive test for all ethnic groups.
Each year, millions of unsuspecting couples are at risk for conceiving a child with a serious genetic disease, such as cystic fibrosis, spinal muscular atrophy, or Tay-Sachs disease.
This is my: 100 a new all in one universal screening test for anyone who wishes to know the risks prior to conception.
This new test offer by this is my: clinic is new to the UK and allows you to prevent needless suffering from the unknown. If you and your partner take the this is my: 100 Genetic Test and test positive, rest assured there are actions you can take to have a healthy baby at which every step of the way you are at.
Before Pregnancy
• Preimplantation Genetic Diagnosis (PGD)
• Donor Egg or Sperm
• Mental Preparation
During Pregnancy
• Watchful Waiting
After Pregnancy
• Early Childhood Treatment
While these diseases cannot be cured, with the this is my: 100 they can now be prevented. The test is recommended to be offered to both men and women and tests for diseases common to every ethnic group, for maximum safety.
While these diseases cannot be cured, with the this is my: 100 they can now be prevented. The test is recommended to be offered to both men and women and tests for diseases common to every ethnic group, for maximum safety.
Diseases covered by the revolutionary new test are listed below:
ABCC8-Related Hyperinsulinism
Achromatopsia
Alkaptonuria
Alpha-1 Antitrypsin Deficiency
Alpha-Mannosidosis
Andermann Syndrome
ARSACS
Aspartylglycosaminuria
Ataxia With Vitamin E Deficiency
Ataxia-Telangiectasia
Autosomal Recessive Polycystic Kidney Disease
Bardet-Biedl Syndrome, BBS1-Related
Bardet-Biedl Syndrome, BBS10-Related
Beta Thalassemia
Biotinidase Deficiency
Bloom Syndrome
Canavan Disease
Carnitine Palmitoyltransferase IA Deficiency
Carnitine Palmitoyltransferase II Deficiency
Cartilage-Hair Hypoplasia
Choroideremia
Citrullinemia Type 1
CLN3-Related Neuronal Ceroid Lipofuscinosis
CLN5-Related Neuronal Ceroid Lipofuscinosis
Cohen Syndrome
Congenital Disorder of Glycosylation Type Ia
Congenital Disorder of Glycosylation Type Ib
Congenital Finnish Nephrosis
Costeff Optic Atrophy Syndrome
Cystic Fibrosis
Cystinosis
D-Bifunctional Protein Deficiency
*Factor V Leiden Thrombophilia
Factor XI Deficiency
Familial Dysautonomia
Familial Mediterranean Fever
Fanconi Anemia Type C
Galactosemia
Gaucher Disease
GJB2-Related DFNB 1 Nonsyndromic Hearing Loss and Deafness
*Glucose-6-Phosphate Dehydrogenase Deficiency
Glutaric Acidemia Type 1
Glycogen Storage Disease Type Ia
Glycogen Storage Disease Type Ib
Glycogen Storage Disease Type III
Glycogen Storage Disease Type V
GRACILE Syndrome
Hereditary Fructose Intolerance
Hereditary Thymine-Uraciluria
Herlitz Junctional Epidermolysis Bullosa, LAMA3-Related
Herlitz Junctional Epidermolysis Bullosa, LAMB3-Related
Herlitz Junctional Epidermolysis Bullosa, LAMC2-Related
Hexosaminidase A Deficiency
*HFE-Associated Hereditary Hemochromatosis
Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency
Hurler Syndrome
Hypophosphatasia, Autosomal Recessive
Inclusion Body Myopathy 2
Isovaleric Acidemia
Joubert Syndrome 2
Krabbe Disease
Limb-Girdle Muscular Dystrophy Type 2D
Limb-Girdle Muscular Dystrophy Type 2E
Lipoamide Dehydrogenase Deficiency
Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Maple Syrup Urine Disease Type 1B
Medium Chain Acyl-CoA Dehydrogenase Deficiency
Megalencephalic Leukoencephalopathy With Subcortical Cysts
Metachromatic Leukodystrophy
*MTHFR Deficiency
Mucolipidosis IV
Muscle-Eye-Brain Disease
NEB-Related Nemaline Myopathy
Niemann-Pick Disease Type C
Niemann-Pick Disease, SMPD1-Associated
Nijmegen Breakage Syndrome
Northern Epilepsy
Pendred Syndrome
PEX1-Related Zellweger Syndrome Spectrum Phenylalanine Hydroxylase Deficiency
Polyglandular Autoimmune Syndrome Type 1
Pompe Disease
PPT1-Related Neuronal Ceroid Lipofuscinosis
Primary Carnitine Deficiency
Primary Hyperoxaluria Type 1
Primary Hyperoxaluria Type 2
PROP1-Related Combined Pituitary Hormone Deficiency
*Prothrombin Thrombophilia
Pseudocholinesterase Deficiency
Pycnodysostosis
Rhizomelic Chondrodysplasia Punctata Type 1
Salla Disease
Segawa Syndrome
Short Chain Acyl-CoA Dehydrogenase Deficiency
Sickle Cell Disease
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophy
Steroid-Resistant Nephrotic Syndrome
Sulfate Transporter-Related Osteochondrodysplasia
Tay-Sachs Disease
TPP1-Related Neuronal Ceroid Lipofuscinosis
Tyrosinemia Type I
Usher Syndrome Type 1F
Usher Syndrome Type 3
Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Wilson Disease
X-Linked Juvenile Retinoschisis
* – Only included if requested by ordering physician.
