Fraser Syndrome Latest Advances

Journal: Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia

Published: February 21, 2023

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

Journal: Diagnostics (Basel, Switzerland)

Published: February 13, 2023

Prenatal hydrometrocolpos as an unusual finding in Fraser syndrome. Case report.

Journal: Case reports in perinatal medicine

Published: November 15, 2022

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MOTA syndrome diagnosis following unexpected neonatal death.

MOTA syndrome diagnosis following unexpected neonatal death.

Fraser Syndrome: A Narrative Review Based on a Case from Vietnam and the Past 20 Years of Research.

Fraser Syndrome: A Narrative Review Based on a Case from Vietnam and the Past 20 Years of Research.

Frem2 knockout mice exhibit Fraser syndrome phenotypes and neonatal lethality due to bilateral renal agenesis.

Frem2 knockout mice exhibit Fraser syndrome phenotypes and neonatal lethality due to bilateral renal agenesis.

Frem2 Knockout Mice Exhibit Fraser Syndrome Phenotypes and Neonatal Lethality Due to Bilateral Renal Agenesis.

Frem2 Knockout Mice Exhibit Fraser Syndrome Phenotypes and Neonatal Lethality Due to Bilateral Renal Agenesis.

Fraser syndrome with limb reduction defect: a rare and unique anatomic variation.

Fraser syndrome with limb reduction defect: a rare and unique anatomic variation.

The Fraser complex interconnects tissue layers to support basal epidermis and osteoblast integrated morphogenesis underlying fin skeletal patterning.

The Fraser complex interconnects tissue layers to support basal epidermis and osteoblast integrated morphogenesis underlying fin skeletal patterning.

Bilateral cryptophthalmos with overlapping features of Manitoba oculo-tricho-anal (MOTA) syndrome and Fraser syndrome 2.

Bilateral cryptophthalmos with overlapping features of Manitoba oculo-tricho-anal (MOTA) syndrome and Fraser syndrome 2.

Oral and Craniofacial Anomalies of Fraser Syndrome:Prosthetic Management.

Oral and Craniofacial Anomalies of Fraser Syndrome:Prosthetic Management.

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal-Epidermal Junction of Mouse Skin.

About a case of Fraser syndrome. Autopsy of a 37 weeks gestation fetus with multiple malformations

About a case of Fraser syndrome. Autopsy of a 37 weeks gestation fetus with multiple malformations

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas.

Prenatal hydrometrocolpos as an unusual finding in Fraser syndrome. Case report.

Prenatal hydrometrocolpos as an unusual finding in Fraser syndrome. Case report.