Genetics, Fertility and Pregnancy - Blog - IntroLab Laboratorija Beograd

Genetics, Fertility and Pregnancy

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What is spinal muscular atrophy and how is it recognized?

Spinal muscular atrophy (SMA) is a rare, inherited neuromuscular disorder caused by a mutation in the SMN1 gene, leading to…

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Male Infertility: Causes, Symptoms and Treatment Options

For many couples, the path to parenthood is not easy. When pregnancy does not occur for a long time, feelings…

Parents looking at their baby’s ultrasound.

Prader Willi Syndrome: Causes, Symptoms, and Treatment Options

Prader Willi syndrome is a rare genetic disorder that affects multiple body systems and causes physical, mental, and behavioral changes.…

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Angelman Syndrome

When a child does not reach expected developmental milestones, parents face a number of questions and uncertainties. Some children start…

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What is X-linked hypophosphatemia?

X-linked hypophosphatemia (XLH) is a rare inherited disease that affects approximately one in 20,000 to 60,000 children born each year.…

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Klinefelter syndrome – a genetic disorder that often goes undetected

Klinefelter syndrome is a common yet often unrecognized chromosomal disorder that can affect development, fertility, and overall health in men.…

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Turner syndrome – How to recognize it and why early diagnosis matters

Turner syndrome is a genetic condition that affects only females and occurs when all or part of one X chromosome…

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What is Edwards Syndrome (Trisomy 18)?

Edwards syndrome is a severe genetic disorder that can have significant health consequences for a baby. For expecting parents, having…

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What is Down syndrome and how does it occur?

Down syndrome (Trisomy 21) is one of the most common genetic disorders, resulting from the presence of an extra copy…

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Thrombophilia and Pregnancy: What You Need to Know

Thrombophilia can present challenges during pregnancy for many women, as this condition increases the risk of complications, including miscarriages, preeclampsia,…