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Higher Human Biology Subtopic 12 Ante and postnatal screening

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Presentation on theme: "Higher Human Biology Subtopic 12 Ante and postnatal screening"— Presentation transcript:

1 Higher Human Biology Subtopic 12 Ante and postnatal screening
Physiology and Health Higher Human Biology Subtopic 12 Ante and postnatal screening

2 Learning Intentions To explain the use of antenatal screening in the identification of disorders To describe antenatal screening techniques To discuss the effects on the Rhesus antigen in pregnancy

3 Antenatal care Carried out to monitor the health of the mother and foetus during pregnancy. Checks include : Height and weight Blood pressure Blood type Urine General health

4 Antenatal screening This can identify the risk of a disorder so that further tests can be carried out and a diagnosis given.

5 Screening Vs Diagnostic Tests
Screening Test Detects signs and symptoms associated with a disorder Assesses the degree of risk Diagnostic test Definite test which establishes, without doubt, whether a person is suffering from a specific condition or disorder

6 Methods of Antenatal Screening
Ultrasound imaging Biochemical tests Diagnostic testing Rhesus antibody testing Video

7 Ultrasound A scanner picks up high-frequency sound that bounce off the foetus and create a picture. Dating Scan 8-14 weeks Determines the stage of pregnancy Used to calculate due date alongside biochemical tests Anomaly Scan 18-20 weeks Can detect physical abnormalities

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9 Biochemical tests Test blood and urine to detect the normal physiological changes of pregnancy. Used to detect : Hypertension Gestational diabetes Anaemia Hyperthyroidism

10 Biochemical tests A women is offered tests at weeks to check for 3 markers. A high / low concentration of a marker chemical can differ depends on the stage of pregnancy.

11 Markers HCG Normally increases wk 6-10 then decreases to a steady low level If it remains high it may be a sign of Down’s syndrome Measuring a substance at the wrong time could lead to a false positive / negative result

12 Diagnostic Tests Offered if : Routine screening has raised a problem
There is a family history of genetic disorders The women is in a high risk category (e.g 35yrs +) 2 main types of test : Amniocentesus CVS

13 Amniocentesus Weeks 14 – 16 Small amount of amniotic fluid taken.
Foetal cells cultured and a karyotype is produced. A karyotype shows chromosome abnormalities.

14 Normal Karyotypes

15 Down’s Syndrome

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17 Kleinfelter's Syndrome
One extra X chromosome

18 Turner’s Syndrome Only 1 X chromosome

19 CVS Chorionic villus sampling Sample of placental cells taken
Karyotype produced Increases the risk of miscarriage but can be carried out earlier in pregnancy

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22 Rhesus Factor A cell marker found on red blood cells
People with the marker are Rh +ve People without it are Rh –ve and have anti-D antibodies which will destroy any Rh +ve cells.

23 During pregnancy… 1st pregnancy
A rh –ve mother will produce anti-D antibodies if she comes into contact with her Rh +ve baby …….sensitisation 2nd pregnancy Her anti-D antibodies will cross the placenta and attach a Rh +ve foetus

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26 Treatment The mother can be given anti-D antibodies to destroy Rh antigens before her immune system kicks in. The fetus can be given a blood transfusion to replace Rh +ve blood with Rh -ve

27 Post natal screening Screening that takes place after birth
PKU is one of a few inherited disorders that can be successfully treated PKU is an inborn error of metabolism

28 × × × × × × Phenylketonuria (PKU)
The amino acid phenylalanine is found in the diet. × enzyme C × × × melanin (Skin pigment ) × Intermediate metabolites enzyme B enzyme A × phenylalanine tyrosine (an amino acid) In a PKU sufferer the gene that codes for enzyme 1 is defective – what will this result in? Phenylalanine builds up in the blood.

29 Phenylketonuria (PKU)
Autosomal recessive Phenylalanine builds up causes mental development to be restricted PKU is routinely tested for in newly born babies using a Heel prick test. Treated by following a low phenylalanine diet

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31 × PKU Albinism Sufferers have lighter skin.
enzyme C melanin (Skin pigment ) Intermediate metabolites enzyme B tyrosine (an amino acid) Albinism Albinos cannot make enzyme so don’t produce melanin

32 Learning Intentions To explain the use of antenatal screening in the identification of disorders To describe antenatal screening techniques To discuss the effects on the Rhesus antigen in pregnancy


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