Dictionary
Acrocephalosyndactyly: Genetics and Phenotype
Acrocephalosyndactyly is a group of rare genetic disorders characterized by craniosynostosis and syndactyly, primarily caused...
Pediatrics
19 results
Dictionary
Acrocephalopolysyndactyly: Clinical Spectrum
Acrocephalopolysyndactyly is a rare genetic condition characterized by craniosynostosis, polysyndactyly, and systemic anomalies, primarily classified...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Achondroplasia: Genetic Insights & Care
Explore an academic overview of achondroplasia, detailing its FGFR3 genetic basis, molecular pathophysiology, clinical features,...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Achiria: Congenital Absence of the Hands
Achiria is a rare congenital anomaly marked by the complete absence of one or both...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Absence Seizure: The Silent Disruption
A detailed academic analysis of absence seizures, examining thalamocortical pathophysiology, 3 Hz spike-and-wave EEG hallmarks,...
October 5, 2026
•
Dr. Mohammed Looti
Dictionary
Abdominal Migraine: The Gut-Brain Dilemma
Abdominal migraine is a pediatric episodic syndrome characterized by recurrent attacks of severe midline abdominal...
October 5, 2026
•
Dr. Mohammed Looti
Scales
Van Wiechen Examination
The Van Wiechen Examination is the standardized national neurodevelopmental screening and surveillance instrument utilized across...
September 12, 2026
•
Dr. Mohammed Looti