Family Planning Screen

LEARN IF YOU OR YOUR PARTNER

CARRY GENETIC DISEASES.

Protect Your Family, Right From the Start.

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Comprehensive

Risk profile for 100+ potential conditions

Genetic Counseling

Complimentary genetic counselors

RESULTS YOU CAN TRUST

State-of-art NGS sequencing technology

Family Planning Screen

Are you thinking about starting a family, or expecting a new addition?

Our family planning screening products help assess the risk of you or your partner passing down genetic conditions that could affect your family by analyzing the risk profile of more than 100 potential conditions based on your genes. Prenetics will provide you complimentary access to genetic counselors who will be available to answer any questions you may have.


Family Planning Screen explained

You and/or your partner may be carriers of genetic conditions without knowing about it. If both of you are carriers for a certain condition, there is a 25% chance that your baby could develop a condition. Some of these conditions have early treatment options, while others may require life-long care.

Based on your risk profile, Prenetics provides specific recommendations to help parents think about how and when to take measures to maximize the health of their expanding family. Knowing your risk profile before or early in a pregnancy allows you to consider your options with time to make choices together with your healthcare provider.

WHAT WE ARE TESTING

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Family Planning Screen is a non-invasive screening for health conditions such as Wilson's disease, cystic fibrosis, and Bloom syndrome that could be passed on to your child. The screening could be done before or during conception. Knowing your risk allows you to prepare and discuss your options with your partner and healthcare provider before delivery.

Over 100 conditions are tested from a simple saliva sample using advanced technology. Once the results are ready, you will have secure access the comprehensive report on both our website and mobile app. Prenetics’ genetic counselors are also available to answer any questions you may have.

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21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia
ABCC8-related Hyperinsulinism
Achondrogenesis Type 1B
Achromatopsia
Alkaptonuria
Alpha Thalassemia
Alpha-1 Antitrypsin Deficiency
Alpha-Mannosidosis
Alpha-Sarcoglycanopathy
Andermann Syndrome
ARSACS
Aspartylglycosaminuria
Ataxia With Vitamin E Deficiency
Ataxia-Telangiectasia
Bardet-Biedl Syndrome, BBS1-related
Bardet-Biedl Syndrome, BBS10-related
Beta-Sarcoglycanopathy
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
Diastrophic Dysplasia
Dihydropyrimidine Dehydrogenase Deficiency
Factor V Leiden Thrombophilia
Factor XI Deficiency
Familial Dysautonomia
Familial Mediterranean Fever
Fanconi Anemia Type C
FKTN-related Disorders
Fragile X Syndrome
Galactosemia
Gaucher Disease
GJB2-related DFNB1 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
HADHA-related Disorders
Hb Beta Chain-Related Hemoglobinopathy (Including Beta Thalassemia and Sickle Cell Disease)
Hereditary Fructose Intolerance
Herlitz Junctional Epidermolysis Bullosa, LAMA3-related
Herlitz Junctional Epidermolysis Bullosa, LAMB3-related
Herlitz Junctional Epidermolysis Bullosa, LAMC2-related
Hexosaminidase A Deficiency (Including Tay-Sachs Disease)
HFE-associated Hereditary Hemochromatosis
Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency
Hypophosphatasia, Autosomal Recessive
Inclusion Body Myopathy 2
Isovaleric Acidemia
Joubert Syndrome 2
Krabbe Disease
Lipoamide Dehydrogenase Deficiency
Maple Syrup Urine Disease Type 1B
Medium Chain Acyl-CoA Dehydrogenase Deficiency
Megalencephalic Leukoencephalopathy With Subcortical Cysts
Metachromatic Leukodystrophy
Mild Hyperhomocysteinemia Caused by MTHFR Deficiency
Mucolipidosis IV
Mucopolysaccharidosis Type I
Muscle-Eye-Brain Disease
NEB-related Nemaline Myopathy
Niemann-Pick Disease Type C
Niemann-Pick Disease, SMPD1-associated
Nijmegen Breakage Syndrome
Northern Epilepsy
PCDH15-related Disorders
Pendred Syndrome
PEX1-related Zellweger Syndrome Spectrum
Phenylalanine Hydroxylase Deficiency
PKHD1-related Autosomal Recessive Polycystic Kidney Disease
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
Recessive Multiple Epiphyseal Dysplasia
Rhizomelic Chondrodysplasia Punctata Type 1
Salla Disease
Segawa Syndrome
Short Chain Acyl-CoA Dehydrogenase Deficiency
Sjogren-Larsson Syndrome
Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophy
Steroid-Resistant Nephrotic Syndrome
Sulfate Transporter-Related Osteochondrodysplasia
TPP1-related Neuronal Ceroid Lipofuscinosis
Tyrosinemia Type I
Usher Syndrome Type 3
Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Wilson Disease
X-Linked Juvenile Retinoschisis

*Must be specifically requested to be included on your panel.