Haematology & Haemato-oncology Clinic
The haematology and haematooncology clinic is held every Thursday from 9.00 am to 12.00 noon Those seen in this clinic include patients with,
- Thalassaemaia
- Haemophilia
- Leukaemias
- Haemachromotosis
- Polycythemia
- And all other haematological and haematooncological conditions
Ophthalmogenetics Clinic
The ophthalmogenetics clinic is held every Friday from 9.00am to 12.00 noon.
Children and adults with congenital and inherited opthlmological conditions are seen in the clinic.
SKELETAL DYSPLASIA CLINIC
The clinic is designed to identify individuals that appear to have familial or hereditary bone dysplasia with or without dysmorphic features, and provide a thorough evaluation of the condition, genetic counseling and education which will be beneficial for the patients and their families. Working in concert with the patients’ physicians, Surgeons and Radiologist will give more benefits for the patients to get better view and understanding of their disabilities.
The services you get Individualized risk assessment for all forms of skeletal dysplasia considering systematic approach. Arrange Screening facilities from reputed reference labs local and Overseas. Genetic counseling for affected families Patient education Indications for Referral
Congenital skeletal dysplasia patients (isolated cases)
Skeletal dysplasias occurring in multiple generations. Two or more close relatives (1st or 2nd degree relatives) with the same deformity or dysplasia. Multiple deformities in a individual.
Diagnosed skeletal dysplasia in a family member. In addition to the above mentioned specific indications, If any person having a relative with skeletal dysplasia may seek the services of the clinic.
Tests for Achondroplasia is currently available. We plan to introduce more tests in the near future with your Demand and Request.
You are welcome to direct Your referrals To
Skeletal dysplasia Genetics Clinic,
Human Genetics Unit,
Faculty of Medicine,
University of Colombo,
Kynsey Road,
Colombo 08
On Every Monday From 08:00am to 04:00pm
Please call/e-mail to book an appointment prior to sending patients for better care.
Telephone: 0112629710
Email: director@genetics.cmb.ac.lk
Cytogenetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Peripheral Blood Karyotyping | 3ml Blood (Sodium Heparin) | Rs. 10,000/- | 28 Days |
Molecular Genetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Genetic Thrombophilia Screen -(Factor V 1691G>A, Prothrombin 20210G>A, MTHFR 677C>T) | 3ml Blood (K.EDTA) | Rs. 8,000/- | 14 Days |
| Factor V 1691G>A (Leiden) Mutation | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Prothrombin 20210G>A Mutation (Factor II) | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Methylene tetrahydrofolate reductase (MTHFR) 677 C>T Mutation | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Detection of the JAK 2 V617F Mutation | 3ml Blood (K.EDTA) | Rs. 6,000/- | 14 Days |
| Hereditary Haemochromatosis – HFE C282Y and H63D Mutations | 3ml Blood (K.EDTA) | Rs. 6,000/- | 14 Days |
| Beta Thalassaemia Common Sri Lankan Mutation screening (HBB) | 3ml Blood (K.EDTA) | Free | 28 Days |
| Alpha Thalassaemia Deletion screening (HBA) common | 3ml Blood (K.EDTA) | Free | 28 Days |
| SRY Gene Detection | 3ml Blood (K.EDTA) | Rs. 6,000/- | 7 Days |
| Y-Chromosome Microdeletion Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
FISH
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Detection of 22q11 Deletion (DiGeorge syndrome) | 3ml Blood (Sodium Heparin) | Rs. 20,000/- | 14 Days |
New-born Screening
| Panel | Code | Disorders | Price |
|---|---|---|---|
| Hb+FS+ | Hb+FS+ | 57 Disorders | Rs. 12,000/- |
| FS+ | FS+ | 51 Disorders | Rs. 11,000/- |
| FS | FS | 49 Disorders | Rs. 10,500/- |
| MS | MS | 45 Disorders | Rs. 8,500/- |
| Bio6 | B6 | 6 Disorders | Rs. 5,000/- |
| Bio5 | B5 | 5 Disorders | Rs. 4,000/- |
| Bio4 | B4 | 4 Disorders | Rs. 3,000/- |
| Hb+ | Hb+ | 4 Disorders | Rs. 1,500/- |
Please refer to the NeoGen_Price_Panel_LKR- 30. 08.2013NeoGen Labs Leaflet for screening panel descriptions & pricing
Cytogenetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Peripheral Blood Karyotyping | 3ml Blood (Sodium Heparin) | Rs. 10,000/- | 28 Days |
Molecular Genetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Genetic Thrombophilia Screen -(Factor V 1691G>A, Prothrombin 20210G>A, MTHFR 677C>T) | 3ml Blood (K.EDTA) | Rs. 4,500/- | 14 Days |
| Factor V 1691G>A (Leiden) Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Prothrombin 20210G>A Mutation (Factor II) | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Methylene tetrahydrofolate reductase (MTHFR) 677 C>T Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Detection of the JAK 2 V617F Mutation | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Hereditary Haemochromatosis – HFE C282Y and H63D Mutations | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
| Beta Thalassaemia Common Sri Lankan Mutation screening (HBB) | 3ml Blood (K.EDTA) | Free | 28 Days |
| Alpha Thalassaemia Deletion screening (HBA) common | 3ml Blood (K.EDTA) | Free | 28 Days |
| SRY Gene Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 7 Days |
| Y-Chromosome Microdeletion Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
FISH
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Detection of 22q11 Deletion (DiGeorge syndrome) | 3ml Blood (Sodium Heparin) | 14 Days |
New-born Screening
| Panel | Code | Disorders | Price |
|---|---|---|---|
| Hb+FS+ | Hb+FS+ | 57 Disorders | Rs. 12,000/- |
| FS+ | FS+ | 51 Disorders | Rs. 11,000/- |
| FS | FS | 49 Disorders | Rs. 10,500/- |
| MS | MS | 45 Disorders | Rs. 8,500/- |
| Bio6 | B6 | 6 Disorders | Rs. 5,000/- |
| Bio5 | B5 | 5 Disorders | Rs. 4,000/- |
| Bio4 | B4 | 4 Disorders | Rs. 3,000/- |
| Hb+ | Hb+ | 4 Disorders | Rs. 1,500/- |
Please refer to the NeoGen_Price_Panel_LKR- 30. 08.2013NeoGen Labs Leaflet for screening panel descriptions & pricing
Cytogenetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Peripheral Blood Karyotyping | 3ml Blood (Sodium Heparin) | Rs. 7,500/- | 28 Days |
Molecular Genetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Genetic Thrombophilia Screen -(Factor V 1691G>A, Prothrombin 20210G>A, MTHFR 677C>T) | 3ml Blood (K.EDTA) | Rs. 4,500/- | 14 Days |
| Factor V 1691G>A (Leiden) Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Prothrombin 20210G>A Mutation (Factor II) | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Methylene tetrahydrofolate reductase (MTHFR) 677 C>T Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Detection of the JAK 2 V617F Mutation | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Hereditary Haemochromatosis – HFE C282Y and H63D Mutations | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
| Beta Thalassaemia Common Sri Lankan Mutation screening (HBB) | 3ml Blood (K.EDTA) | Free | 28 Days |
| Alpha Thalassaemia Deletion screening (HBA) common | 3ml Blood (K.EDTA) | Free | 28 Days |
| SRY Gene Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 7 Days |
| Y-Chromosome Microdeletion Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
FISH
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Detection of 22q11 Deletion (DiGeorge syndrome) | 3ml Blood (Sodium Heparin) | 14 Days |
New-born Screening
| Panel | Code | Disorders | Price |
|---|---|---|---|
| Hb+FS+ | Hb+FS+ | 57 Disorders | Rs. 12,000/- |
| FS+ | FS+ | 51 Disorders | Rs. 11,000/- |
| FS | FS | 49 Disorders | Rs. 10,500/- |
| MS | MS | 45 Disorders | Rs. 8,500/- |
| Bio6 | B6 | 6 Disorders | Rs. 5,000/- |
| Bio5 | B5 | 5 Disorders | Rs. 4,000/- |
| Bio4 | B4 | 4 Disorders | Rs. 3,000/- |
| Hb+ | Hb+ | 4 Disorders | Rs. 1,500/- |
Please refer to the NeoGen_Price_Panel_LKR- 30. 08.2013NeoGen Labs Leaflet for screening panel descriptions & pricing
Cytogenetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Peripheral Blood Karyotyping | 3ml Blood (Sodium Heparin) | Rs. 7,500/- | 28 Days |
Molecular Genetics Testing
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Genetic Thrombophilia Screen -(Factor V 1691G>A, Prothrombin 20210G>A, MTHFR 677C>T) | 3ml Blood (K.EDTA) | Rs. 4,500/- | 14 Days |
| Factor V 1691G>A (Leiden) Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Prothrombin 20210G>A Mutation (Factor II) | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Methylene tetrahydrofolate reductase (MTHFR) 677 C>T Mutation | 3ml Blood (K.EDTA) | Rs. 1,500/- | 14 Days |
| Detection of the JAK 2 V617F Mutation | 3ml Blood (K.EDTA) | Rs. 3,500/- | 14 Days |
| Hereditary Haemochromatosis – HFE C282Y and H63D Mutations | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
| Beta Thalassaemia Common Sri Lankan Mutation screening (HBB) | 3ml Blood (K.EDTA) | Free | 28 Days |
| Alpha Thalassaemia Deletion screening (HBA) common | 3ml Blood (K.EDTA) | Free | 28 Days |
| SRY Gene Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 7 Days |
| Y-Chromosome Microdeletion Detection | 3ml Blood (K.EDTA) | Rs. 4,000/- | 14 Days |
FISH
| Test Name | Specimen/ Container | Cost | Reporting Time |
|---|---|---|---|
| Detection of 22q11 Deletion (DiGeorge syndrome) | 3ml Blood (Sodium Heparin) | 14 Days |
New-born Screening
| Panel | Code | Disorders | Price |
|---|---|---|---|
| Hb+FS+ | Hb+FS+ | 57 Disorders | Rs. 12,000/- |
| FS+ | FS+ | 51 Disorders | Rs. 11,000/- |
| FS | FS | 49 Disorders | Rs. 10,500/- |
| MS | MS | 45 Disorders | Rs. 8,500/- |
| Bio6 | B6 | 6 Disorders | Rs. 5,000/- |
| Bio5 | B5 | 5 Disorders | Rs. 4,000/- |
| Bio4 | B4 | 4 Disorders | Rs. 3,000/- |
| Hb+ | Hb+ | 4 Disorders | Rs. 1,500/- |
Please refer to the NeoGen_Price_Panel_LKR- 30. 08.2013NeoGen Labs Leaflet for screening panel descriptions & pricing
- Patient Information Sheet Page1 [PDF]
- Patient Information Sheet Page2 [PDF]
- Patient Information Sheet (Neurology) [PDF]
- Request Form For Molecular Genetic Testing (Thrombophilia) [PDF]
- Request Form For Molecular Genetic Testing (Thalassaemia) [PDF]
- Request Form For Molecular Genetic Testing (Jak 2 – Mpn) [PDF]
- Consent Form For Genetic Testing: Sinhala [PDF] | Tamil [PDF] | English[PDF]
- Consent Form For Clinical Photography/ Video: Sinhala [PDF] | Tamil [PDF] | English[PDF]
- Skeletal Dysplasia Clinic – Patients Referral Form [PDF]