Warmblood fragile foal syndrome type 1 mutation ( PLOD1 c.2032G>A) is not associated with catastrophic breakdown and has a low allele frequency in the Thoroughbred breed

Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome

BACKGROUND Skin malformations that resembled manifestations of Ehlers-Danlos-Syndrome were described in a variety of domestic animals during the last century as cutis hyperelastica, hyperelastosis cutis, dermatosparaxis, dermal/collagen dysplasia, dermal/cutaneous asthenia or Ehlers-Danlos-like syndrome/s. In 2007, the mutation responsible for Hereditary Equine Regional Dermal Asthenia (HERDA) ...

A Novel Splice Site Mutation in HPS1 Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family

Vitamin D Deficiency is Associated with the Metabolic Syndrome in Subjects with Type 2 Diabetes

Background and Objectives: There is convincing evidence that subjects concomitantly affected by type 2 diabetes (T2D) and metabolic syndrome (MeS) are at greater risk for cardiovascular disease (CVD). Many metabolic derangements in T2D might be attributed to poor vitamin D status. The purpose of this study was to investigate the associations among vitamin D status, MeS and glycemic status in su...

the past hospitalization and its association with suicide attempts and ideation in patients with mdd and comparison with bmd (depressed type) group

چکیده ندارد.

Small colon faecalith impaction in a thoroughbred foal

An 8-month-old female thoroughbred foal was presented showing signs of colic. The foal was anxious,exhibiting signs of abdominal pain and distention. The foal had tachycardia (120 beats/min), tachypnea (40breaths/min). Blood samples obtained for haematologic and serum biochemistry analysis that showed a PCVof 30% and a TPP of 70 g/L. The peritoneal fluid analysis revealed a clear fluid with mil...