ADPKD
Autosomal dominant polycystic kidney disease overview, diagnosis, family screening, and monitoring.
Inherited kidney disease care
Precision kidney genetics with human warmth.
KidGene brings together clinical assessment, genetic counseling, family screening, long-term monitoring, and research for patients and families affected by inherited kidney disease.
A calm bilingual direction for patients, families, physicians, researchers, donors, and the public.
Many inherited kidney diseases are underdiagnosed. Early recognition can help protect patients and families through appropriate diagnosis, monitoring, and counseling.
Clinical service - Education - Research
Clean, calm, and precise.
Designed around the KidGene green, gold, sage, and champagne identity.
How can we help you?
Clear pathways for every visitor.
The homepage routes patients, families, doctors, learners, researchers, and donors to the right journey without feeling crowded.
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I am a patient
Learn who should visit, what to prepare, and what care may involve.
I am family
Understand family screening, inheritance, counseling, and long-term planning.
I am a doctor
Referral indications, required documents, and clinical tools.
I want to learn
Patient-friendly disease information and genetic testing basics.
I want to donate
Support diagnosis, education, counseling, awareness, and research.
About KidGene
A national and regional center for inherited kidney disease care.
The center improves diagnosis, care, education, and research through integrated clinical service, genetic evaluation, family-based care, and patient-centered education.
1Clinical care for inherited kidney diseases
2Genetic counseling and family-based care
3Diagnosis, risk assessment, and follow-up
4Awareness for patients, families, and professionals
Patient care
Supportive care from first suspicion to long-term follow-up.
This section should feel calm, reassuring, and practical, with simple language for patients and families.
Referral or appointment request
Patient is referred by a physician or contacts the center.
Initial assessment
Medical history, family history, laboratory review, imaging review, and examination.
Genetic counseling
Explanation of possible benefits, limitations, risks, family implications, and consent.
Testing and interpretation
Gene panel, exome, genome, or copy-number analysis may be considered when appropriate.
Family screening and follow-up
Long-term plan for the patient and relatives who may benefit from screening or counseling.
Disease information
Patient-friendly education with physician-level credibility.
Use short pages first, then expand into bilingual handouts, videos, FAQs, and patient stories after approval.
Alport syndrome
Kidney, hearing, and eye features with inheritance patterns and family evaluation.
Fabry disease
Rare multisystem disease with kidney involvement and treatment implications.
CAKUT
Congenital anomalies of the kidney and urinary tract with genetic considerations.
Tubulopathies
Inherited tubular disorders affecting salt, mineral, acid-base, and water balance.
Genetic FSGS
Genetic forms of focal segmental glomerulosclerosis and implications for care.
Genetic testing
Testing should be precise, consented, and clinically useful.
Explain genetic testing in plain language, including what it can and cannot answer, why counseling matters, and how results may affect family members.
ASingle-gene testing, panels, exome, genome, and copy-number analysis
BPre-test counseling, consent, and documentation
CResult interpretation with clinical correlation
DFamily cascade screening when appropriate
For physicians
Make referral criteria easy to understand and act on.
Physician pages should be concise, clinically structured, and optimized for fast referral decisions.
Early-onset CKD, unexplained kidney disease, or syndromic features
Positive family history of kidney disease, hearing loss, cysts, or kidney failure
Suspicion of ADPKD, Alport syndrome, Fabry disease, CAKUT, tubulopathy, or genetic FSGS
Need for genetic counseling before transplant, reproductive planning, or family screening
Referral package
Recommended launch content: referral indications, clinic schedule, required documents, prior labs, imaging, pedigree, and consent process.
01Referral criteria
02Required records
03Testing guidance
04Contact route
Research and registry
A trusted academic identity for discovery and collaboration.
Research pages can later include registry information, participation criteria, collaboration routes, publications, and ongoing studies.
From diagnosis to knowledge.
KidGene can position itself as a center that transforms clinical care into better understanding of inherited kidney disease in Thailand and the region.
1Patient registry development
2Genotype-phenotype studies
3Education and awareness programs
4Local and international collaboration
Donate
Support diagnosis, education, counseling, and research.
Donation messaging should feel transparent, dignified, and institutional. Add official payment details and policies only after hospital approval.
Patient education materials
Genetic counseling support
Awareness programs
Research and registry infrastructure
Contact
Route inquiries clearly before launch.
Use separate contact paths for patients, families, physicians, research collaborators, donors, media, and general questions.
ClinicSiriraj Hospital contact details to be added
EmailOfficial center email to be added
PhoneAppointment and referral numbers to be added
LocationMap and clinic room details to be added