Early‐onset muscle weakness syndrome (<scp>MW</scp>) in an Australian Holstein calf

Early-onset muscle weakness syndrome (MW) is a recessive genetic disorder known to affect Holstein cattle. This report describes the clinical findings in an Australian Holstein calf diagnosed with MW. The calf initially presented for examination at a dairy farm at 3 days of age, being recumbent since birth but able to stand with assistance. A presumptive diagnosis of traumatic injury was made at first. However, the calf was re-examined multiple times due to ongoing intermittent episodes of recumbency, prompting further diagnostic investigation. Given the non-specific nature of the clinical and laboratory findings, a presumptive diagnosis of MW was made after reviewing the calf's breeding pedigree. A definitive diagnosis, however, required genotype testing. To the authors knowledge, this case report represents the first peer-reviewed manuscript to describe the clinical presentation of MW in an Australian Holstein calf.

Authors

Institutions

Publication Details

Journal
Australian Veterinary Journal
Published
2025-03-04
DOI
https://doi.org/10.1111/avj.13431
Primary Topic
Hereditary Neurological Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Early‐onset muscle weakness syndrome (MW) in an Australian Holstein calf

A. Phipps, MG Ciacia
Australian Veterinary Journal
Hereditary Neurological Disorders
article

Early‐onset muscle weakness syndrome (MW) in an Australian Holstein calf

A. Phipps, MG Ciacia
article en

Abstract

Early-onset muscle weakness syndrome (MW) is a recessive genetic disorder known to affect Holstein cattle. This report describes the clinical findings in an Australian Holstein calf diagnosed with MW. The calf initially presented for examination at a dairy farm at 3 days of age, being recumbent since birth but able to stand with assistance. A presumptive diagnosis of traumatic injury was made at first. However, the calf was re-examined multiple times due to ongoing intermittent episodes of recumbency, prompting further diagnostic investigation. Given the non-specific nature of the clinical and laboratory findings, a presumptive diagnosis of MW was made after reviewing the calf's breeding pedigree. A definitive diagnosis, however, required genotype testing. To the authors knowledge, this case report represents the first peer-reviewed manuscript to describe the clinical presentation of MW in an Australian Holstein calf.

Australian Veterinary JournalVol. 103(5)
Charles Sturt University (AU)
Openalex Percentile: Top 95%
Hereditary Neurological Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.