Neurocutaneous Syndromes in Children: Prevalence and Clinical Characteristics

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 18
SponsorAssiut University

About this trial

This cross-sectional study aims to determine the prevalence, clinical characteristics, and management patterns of neurocutaneous syndromes among children attending the Pediatric Neurology Unit at Assiut University.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age from birth to 18 years

Diagnosis of neurocutaneous syndrome according to established clinical and/or genetic diagnostic criteria

Written informed consent from parents or legal guardians

Disqualifiers

Uncertain diagnosis

Incomplete medical records

Refusal of parents or legal guardians to participate

Trial population

Children aged from birth to 18 years diagnosed with neurocutaneous syndromes attending the Pediatric Neurology Unit (outpatient or inpatient) at Assiut University during the study period.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: Single cohort: Children with neurocutaneous syndromes

Trial outcomes

Primary outcomes

1

Prevalence of Neurocutaneous Syndromes Among Pediatric Neurology Patients

Proportion of children diagnosed with neurocutaneous syndromes among all patients attending the Pediatric Neurology Unit during the study period. Prevalence calculated as number of NCS cases divided by total number of pediatric neurology attendees during the same period.

Time frame
Baseline
2

Distribution of Neurofibromatosis Type 1

Frequency and percentage of Neurofibromatosis type 1 among diagnosed neurocutaneous syndrome cases.

Time frame
Baseline
3

Distribution of Neurofibromatosis Type 2

Frequency and percentage of Neurofibromatosis type 2 among diagnosed neurocutaneous syndrome cases.

Time frame
Baseline
4

Distribution of Tuberous Sclerosis Complex

Frequency and percentage of Tuberous Sclerosis Complex among diagnosed neurocutaneous syndrome cases.

Time frame
Baseline

Secondary outcomes

1

Cutaneous Manifestations

Frequency and percentage of cutaneous manifestations among children with neurocutaneous syndromes, assessed by clinical examination.

Time frame
Baseline
2

Epilepsy

Frequency and percentage of epilepsy among children with neurocutaneous syndromes, assessed by clinical examination and EEG.

Time frame
Baseline
3

Developmental Delay

Frequency and percentage of developmental delay among children with neurocutaneous syndromes, assessed by clinical examination.

Time frame
Baseline
4

Intellectual Disability

Frequency and percentage of intellectual disability among children with neurocutaneous syndromes, assessed by clinical examination.

Time frame
Baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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