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Information for Parents

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This information can help healthcare professionals speak with people, following suspected or confirmed diagnosis of exomphalos.

Details

This publication explains the abdominal wall defect exompahlos, a condition also known as omphalocele. The NHS fetal anomaly screening programme ( FASP) tests for this condition.

The document includes information about:

what the condition is

how common it is

how it is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancy

where more support and information is available

Contact the PHE Screening helpdesk with any queries about this publication, making sure you include its full title.

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This information can help healthcare professionals speak with people, following suspected or confirmed diagnosis of exomphalos.

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Information for Parents

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This information can help healthcare professionals speak with people, following suspected or confirmed diagnosis of gastroschisis.

Details

This publication explains the condition gastroschisis, found following an ultrasound pregnancy screen.

This document includes information about:

what the condition is

how common it is

how it is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancy

where more support and information is available

The NHS fetal anomaly screening programme ( FASP) tests for this condition.

Contact the PHE Screening helpdesk with any queries about this publication, making sure you include its full title.

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This information can help healthcare professionals speak with people, following suspected or confirmed diagnosis of gastroschisis.

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Information for Parents

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Bilateral renal agenesis: information for parents

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Information to help healthcare professionals speak with people, following suspected or confirmed diagnosis of bilateral renal agenesis.

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Information for Parents

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This information can help can help parents of babies with suspected or confirmed diagnosis of cleft lip discuss the condition with healthcare professionals.

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Information for Parents

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Congenital Diaphragmatic Hernia: information for parents

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This leaflet can help healthcare professionals speak with people, following suspected or confirmed diagnosis of congenital diaphragmatic hernia (CDH).

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Information for Parents

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Information to help healthcare professionals speak with parents, following suspected or confirmed diagnosis of congenital heart disease.

Details

This publication explains congenital heart disease, a condition screened for using an ultrasound scan as part of the NHS fetal anomaly screening programme ( FASP).

The document explains:

what the condition is

how common it is

how it is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancy

where more support and information is available

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Congenital heart disease: information for parents

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Information to help healthcare professionals speak with parents, following suspected or confirmed diagnosis of congenital heart disease.

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Information for Parents

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This information is for parents whose baby may have Patau's syndrome. It can help them talk through the next stages of their care with health professionals.

Details

Patau's syndrome is a condition screened for at the 20-week scan as part of the NHS Fetal Anomaly Screening Programme (FASP). This document includes information for parents about:

what the condition is

follow-up tests and appointments

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancies

where more support and information is available

Refer to how to print digital leaflets if you need to provide a copy of this guidance to people who cannot access the internet.

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Patau's syndrome (T13): information for parents

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This information is for parents whose baby may have Patau's syndrome. It can help them talk through the next stages of their care with health professionals.

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Information for Parents

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This information is for parents whose baby may have Edwards' syndrome. It can help them talk through the next stages of their care with health professionals.

Details

Edwards' syndrome is a condition screened for at the 20-week scan as part of the NHS Fetal Anomaly Screening Programme (FASP). This document includes information for parents about:

what the condition is

follow-up tests and appointments

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancies

where more support and information is available

Refer to how to print digital leaflets if you need to provide a copy of this guidance to people who cannot access the internet.

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Edwards' syndrome (T18): information for parents

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This information is for parents whose baby may have Edwards' syndrome. It can help them talk through the next stages of their care with health professionals.

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Information for Parents

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Cookies on GOV.UK

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This leaflet is for pregnant women whose baby may have anencephaly. It can help women talk through the next stages of their care with health professionals.

Details

This publication explains the neural tube defect anencephaly, a condition screened for by an ultrasound scan as part of the NHS Fetal Anomaly Screening Programme.

The document includes information for parents whose baby has screened positively for anencephaly about:

what the condition is

how common it is

how it is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancy

where more support and information is available

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This leaflet is for pregnant women whose baby may have anencephaly. It can help women talk through the next stages of their care with health professionals.

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Information for Parents

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Cookies on GOV.UK

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This information can help parents of babies with suspected or confirmed diagnosis of severe skeletal dysplasia discuss the condition with healthcare professionals.

Details

This publication explains severe skeletal dysplasia.

It includes information about:

what the condition is

how common it is

how it is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancy

where more support and information is available

The NHS fetal anomaly screening programme (FASP) tests for this condition.

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Severe skeletal dysplasia: information for parents

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This information can help parents of babies with suspected or confirmed diagnosis of severe skeletal dysplasia discuss the condition with healthcare professionals.

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Information for Parents

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Cookies on GOV.UK

We use some essential cookies to make this website work.

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Information for pregnant women whose baby may have spina bifida, including treatment options.

Details

This leaflet explains spina bifida, a condition screened for by the NHS Fetal Anomaly Screening Programme.

Information in the leaflet includes:

what spina bifida is, and how common it is

how the condition is diagnosed and confirmed

what treatment is available

what the outlook for the baby is

what happens next

how likely it is to happen in future pregnancies

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Information for pregnant women whose baby may have spina bifida, including treatment options.

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Description brief

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Information for pregnant women who are offered a chorionic villus sampling (CVS) or amniocentesis diagnostic test.

Details

CVS and amniocentesis are diagnostic tests that can tell if a baby definitely has a serious condition by checking their chromosomes. This document is for pregnant women who are offered a CVS or amniocentesis test following antenatal screening tests.

This information is available in A4 PDF format (in English) to print out and provide for people who cannot access digital information (see list above).

Contact the Screening helpdesk with any queries about this publication, making sure you include its full title.

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CVS and amniocentesis diagnostic tests: description in brief

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Information for pregnant women who are offered a chorionic villus sampling (CVS) or amniocentesis diagnostic test.