Granuloprival cerebellar cortical degeneration in a mixed breed dog with an EMC1 mutation

A mixed-breed male puppy had a 6-month history of progressive cerebellar ataxia and head tremors without a clinically detectable cause. Euthanasia with a necropsy was elected based on the severity of the puppy's clinical signs and lack of response to treatment. At necropsy, the cerebellum was mildly atrophied, and microscopically there was severe diffuse loss of the cerebellar internal granular cell layer with minimal loss of Purkinje cells (granuloprival degeneration). A novel, heterozygous point mutation in the endoplasmic reticulum membrane protein complex subunit 1 (EMC1) gene was detected via whole genome sequencing. Homozygous and heterozygous EMC1 variants are associated with neurodevelopmental delay and cerebellar atrophy in humans. This is the first report of a canine EMC1 mutation with association to granuloprival cerebellar degeneration and expands the genetic implications of this uncommon phenotype of cerebellar atrophy.

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Publication Details

Journal
Journal of Comparative Pathology
Published
2026-04-30
DOI
https://doi.org/10.1016/j.jcpa.2026.04.009
Primary Topic
Neurological diseases and metabolism
Type
article
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article

Granuloprival cerebellar cortical degeneration in a mixed breed dog with an EMC1 mutation

Laura K. Bryan, Beth Boudreau, Kristen L. Shekelle, Kian Martin
Journal of Comparative Pathology
Neurological diseases and metabolism
article

Granuloprival cerebellar cortical degeneration in a mixed breed dog with an EMC1 mutation

Laura K. Bryan, Beth Boudreau, Kristen L. Shekelle, Kian Martin
article en

Abstract

A mixed-breed male puppy had a 6-month history of progressive cerebellar ataxia and head tremors without a clinically detectable cause. Euthanasia with a necropsy was elected based on the severity of the puppy's clinical signs and lack of response to treatment. At necropsy, the cerebellum was mildly atrophied, and microscopically there was severe diffuse loss of the cerebellar internal granular cell layer with minimal loss of Purkinje cells (granuloprival degeneration). A novel, heterozygous point mutation in the endoplasmic reticulum membrane protein complex subunit 1 (EMC1) gene was detected via whole genome sequencing. Homozygous and heterozygous EMC1 variants are associated with neurodevelopmental delay and cerebellar atrophy in humans. This is the first report of a canine EMC1 mutation with association to granuloprival cerebellar degeneration and expands the genetic implications of this uncommon phenotype of cerebellar atrophy.

Journal of Comparative PathologyVol. 227
Texas A&M University (US)
Good health and well-being
Openalex Percentile: Top 10%
Neurological diseases and metabolism
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