Odontotrichomelic Syndrome Latest Advances

GAPO syndrome: a comprehensive examination and review of 105 clinical cases.

Journal: Journal of medical genetics

Published: April 25, 2025

GAPO syndrome: a novel variant in ANTXR1 gene.

Journal: Ophthalmic genetics

Published: May 01, 2024

Endoscopic Optic Nerve Decompression in a Hamamy Syndrome Patient With Bilateral Optic Canal Stenosis.

Journal: The Journal of craniofacial surgery

Published: March 24, 2024

ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.

Journal: Scientific reports

Published: December 29, 2023

Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review.

Journal: European journal of medical genetics

Published: July 22, 2023

Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings.

Journal: Ophthalmic genetics

Published: February 07, 2023

Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.

Journal: Clinical dysmorphology

Published: September 12, 2022

Dental Management of Siblings with GAPO Syndrome.

Journal: Journal of dentistry for children (Chicago, Ill.)

Published: July 29, 2021

Converging physiological roles of the anthrax toxin receptors.

Journal: F1000Research

Published: August 02, 2019

GAPO syndrome with craniosynostosis and intracranial hypertension.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: May 03, 2019

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.

Journal: American journal of medical genetics. Part A

Published: October 19, 2018

Telogen hair loss and androgenetic-like alopecia in GAPO syndrome.

Journal: The Australasian journal of dermatology

Published: April 10, 2018

Odontotrichomelic Syndrome Latest Advances

Find the Latest Research About Odontotrichomelic Syndrome

GAPO syndrome: a comprehensive examination and review of 105 clinical cases.

GAPO syndrome: a comprehensive examination and review of 105 clinical cases.

GAPO syndrome: a novel variant in ANTXR1 gene.

GAPO syndrome: a novel variant in ANTXR1 gene.

Endoscopic Optic Nerve Decompression in a Hamamy Syndrome Patient With Bilateral Optic Canal Stenosis.

Endoscopic Optic Nerve Decompression in a Hamamy Syndrome Patient With Bilateral Optic Canal Stenosis.

ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.

ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.

Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review.

Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review.

Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings.

Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings.

Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.

Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.

Dental Management of Siblings with GAPO Syndrome.

Dental Management of Siblings with GAPO Syndrome.

Converging physiological roles of the anthrax toxin receptors.

Converging physiological roles of the anthrax toxin receptors.

GAPO syndrome with craniosynostosis and intracranial hypertension.

GAPO syndrome with craniosynostosis and intracranial hypertension.

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.

Telogen hair loss and androgenetic-like alopecia in GAPO syndrome.

Telogen hair loss and androgenetic-like alopecia in GAPO syndrome.