Amna M. Futaisi-Al

Muscat, MA, Oman

Last Updated: 09/26/2026

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Found 32 publications

Parry-Romberg Syndrome With Localized Scleroderma: A Report of Two Pediatric Cases From Oman.

Parry-Romberg Syndrome With Localized Scleroderma: A Report of Two Pediatric Cases From Oman.

Journal: Cureus

Published: October 28, 2025

SLC52A3-related Brown-Vialetto-Van Laere syndrome: a large cohort from the Arabian Peninsula.

SLC52A3-related Brown-Vialetto-Van Laere syndrome: a large cohort from the Arabian Peninsula.

Journal: European journal of human genetics : EJHG

Published: September 06, 2025

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.

Journal: American journal of human genetics

Published: October 08, 2024

Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman.

Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman.

Journal: Global public health

Published: July 25, 2024

Transient response to high-dose niacin therapy in a patient with NAXE deficiency.

Transient response to high-dose niacin therapy in a patient with NAXE deficiency.

Journal: JIMD reports

Published: February 02, 2024

Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder.

Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 18, 2023

Medical Tourism and Neurological Diseases: Omani Patients' Experience Seeking Treatment Abroad.

Medical Tourism and Neurological Diseases: Omani Patients' Experience Seeking Treatment Abroad.

Journal: Oman medical journal

Published: July 29, 2023

Biallelic variants in the synaptic vesicle glycoprotein 2 A are associated with epileptic encephalopathy.

Biallelic variants in the synaptic vesicle glycoprotein 2 A are associated with epileptic encephalopathy.

Journal: European journal of human genetics : EJHG

Published: June 05, 2023

Childhood Absence Epilepsy Associated With Concomitant Centrotemporal Spikes.

Childhood Absence Epilepsy Associated With Concomitant Centrotemporal Spikes.

Journal: Cureus

Published: August 25, 2022

Pediatric Migraines: A Comprehensive Review and Perspectives on Diagnosis and Treatment.

Pediatric Migraines: A Comprehensive Review and Perspectives on Diagnosis and Treatment.

Journal: Oman medical journal

Published: August 23, 2022

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.

Journal: Scientific reports

Published: August 01, 2022

Revisiting Exome Data Identified Missed Splice Site Variant of the Asparagine Synthetase ( ASNS ) Gene.

Revisiting Exome Data Identified Missed Splice Site Variant of the Asparagine Synthetase ( ASNS ) Gene.

Journal: Journal of pediatric genetics

Published: May 10, 2022

Showing 1-12 of 32

Last Updated: 09/26/2026