LFS, or coat color dilution lethal, is a tetanic neurologic syndrome of neonatal foals of Egyptian Arabian breeding. The disease is rare and the outcome is uniformly fatal in affected individuals. The disease is genetic and appears to have an autosomal recessive mode of inheritance.
The CBC is typically unremarkable, unless septicemia develops. Serum biochemistry analysis is usually normal, but it may display evidence that the foal has not nursed its dam or received colostrum (hypoproteinemia, hypoglobulinemia, hypogammaglobulinemia, and hypoglycemia).
Skull and cervical spinal radiography may be performed to rule out congenital bony malformations in these regions, but imaging is not useful for supporting a diagnosis of LFS.
Histopathologic analysis of skin biopsy specimens may reveal melanin clumping and follicular dysplasia in affected individuals.
No gross or histologic lesions of the central nervous system have been noted during postmortem examination of affected foals. Evidence of self-trauma inflicted during paddling and changes associated with recumbency (dependent pulmonary atelectasis, decubital ulceration) are often the only gross postmortem findings. Melanin clumping in the dermal follicular bulbs and hair shafts may be noted histologically.
Affected foals may be referred to a tertiary care facility for evaluation and treatment for neonatal maladjustment syndrome or sepsis. Failure to respond to conventional treatment for these diseases, as well as the characteristic signalment and appearance of these foals, is often sufficiently diagnostic. There is no treatment for LFS, and the prognosis is hopeless for affected individuals.
A lack of response to treatment and recognition of the likely diagnosis based on breed and color should prompt euthanasia in most cases. Genetic testing can confirm the diagnosis antemortem.
Based on the known genetic nature and mode of inheritance of the disorder, it is recommended that genetic testing of Egyptian Arabian breeding stock be performed and carriers removed from breeding programs in an attempt to prevent the disease.
Mares and stallions that have produced affected foals have also produced foals with juvenile epilepsy. The relationship, if any, between these 2 syndromes is not clear, but they do not appear to occur concurrently.
Brooks SA, , , et al. Whole-genome SNP association in the horse: identification of a deletion in myosin Va responsible for lavender foal syndrome. PLoS Genet 2010;6(4):e1000909.
Page P, , , et al. Clinical, clinicopathologic, postmortem examination findings and familial history of 3 Arabians with lavender foal syndrome. J Vet Intern Med 2006;20:14911494.