Startle or Seizure? Telling Your Baby’s Normal Movements from Seizures
Many sudden baby movements are completely normal, but a few can be seizures. We explain the difference simply, when to see a doctor, and…
Read articlePediatric neurology · Inherited metabolic disorders
Specialist care with Dr. Walaa Mohamed El-Naggar, with clear steps that help your family prepare and follow up.
Mind · Care · Growth
Academic & clinical expertise
How can we help?
Choose the area closest to your child’s needs to see how assessment and follow-up work.
Assessment of movement and learning development, and of any change in skills your child already had.
02Review of your child’s history and tests, and follow-up care for inherited metabolic conditions.
03Understanding your child’s seizures, reviewing previous reports and following the right care plan.
04A careful look at your daughter’s development, a clinical assessment and review of genetic reports.
05Explaining genetic reports alongside your child’s examination, and talking through results and next steps.
06Ongoing follow-up of your child’s needs, coordinating medical and therapy steps with your family.
About the doctor
Each visit starts by listening to your child’s history and your observations, followed by a detailed neurodevelopmental exam and a review of imaging, genetic and metabolic results to build a clear care plan.
Care-path guide
Answer 3 short questions to see which reports and tests help before the visit, and the right next step for your family.
For families living outside Egypt
Remote video consultations, genomic (WES) report review and pre-arranged Cairo visits when needed.
MRI, metabolic and genetic reports, reviewed for completeness before the consultation.
A video session with Dr. Walaa to review symptoms, family history and genetic results.
A consultant report covering medication, therapeutic formulas and rehabilitation guidance.
When needed, tests and appointments are arranged before the family arrives.
From your first question to your visit
Send a short request and choose a day that suits your family.
The clinic team reviews your request and contacts you to confirm.
Gather previous reports, your notes and the questions you want to discuss.
The family guide
Many sudden baby movements are completely normal, but a few can be seizures. We explain the difference simply, when to see a doctor, and…
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Read articleFrequently asked questions
Didn’t find your answer? Contact the clinic team and we’ll help.
Contact usWhen there are unexplained seizures or spells, delayed walking or speech, loss of skills your child already had, low muscle tone, or abnormal newborn-screening or genetic results.
Bring MRI reports and discs, EEG reports, previous metabolic and genetic tests, the current medication list with doses, and short videos of any seizures or unusual movements.
Yes. Remote video consultations are available for families living outside Egypt, including genetic (WES) report review, with a coordinated Cairo visit when needed.
It is a genetic test that reads the protein-coding parts of the genes. It is usually requested for developmental regression, drug-resistant seizures or a suspected rare genetic condition after clinical assessment.
Send a short request through the website or call the clinic on +20 105 002 9415. The clinic team reviews your request and contacts you to confirm.
We are here to help
Request a visit, or contact the clinic team if you need help booking.
