Phenotypic diagnosis of dwarfism in six Friesian horses

An extreme form of abnormal development, dwarfism, is common in man and some animals, but has not been officially reported in horses. Within the Friesian horse breed, congenital dwarfism has been recognised for many years, but no detailed report exists on its phenotype. The most salient feature of the dwarf syndrome is the physeal growth retardation in both limbs and ribs. Affected animals have approximately 25% shorter fore- and hindlimbs and approximately 50% reduced bodyweight. Postnatal growth is still possible in these animals, albeit at a slower rate: the head and back grow faster than the limbs and ribs leading to the characteristic disproportional growth disturbance. Thus, adult dwarfs exhibit a normal, but a relatively larger head conformation, a broader chest with narrowing at the costochondral junction, a disproportionally long back, abnormally short limbs, hyperextension of the fetlocks and narrow long-toed hooves. Furthermore, a dysplastic metaphysis of the distal metacarpus and metatarsus is radiographically evident. Microscopic analysis of the growth plates at the costochondral junction shows an irregular transition from cartilage to bone, and thickening and disturbed formation of chondrocyte columns, which is similar to findings in osteochondrodysplasia.     

Achondroplastic dog breeds have no mutations in the transmembrane domain of the FGFR-3 gene.

One of the most common skeletal affections in humans is achondroplasia, a short-limbed dwarfism that is, in most cases, caused by mutations in the transmembrane domain of the fibroblast growth factor receptor-3 (FGFR-3) gene. Due to the lack of sufficient radiological, genetic, and molecular studies, most types of skeletal anomalies in dogs are classified as achondroplasia. To initiate the molecular characterization of some osteochondrodysplastic dog breeds, we obtained the DNA sequence of the transmembrane domain of the FGFR-3 gene from the dachshund, basset hound, bulldog, and German shepherd dogs. All 4 breeds showed no mutation in the evaluated region. This indicates that the mutation responsible for the osteochondrodysplastic phenotype in the tested dog breeds lies either elsewhere in the FGFR-3 gene or in other ones involved in the formation and development of endochondral bone.     

Hypercalcemia and parathyroid hormone-related protein in a dog with undifferentiated nasal carcinoma.

Hypercalcemia was discovered in a 7-year-old, castrated male basset hound with a suspected nasal tumor. The dog died the day after admission and nasal carcinoma and disseminated intravascular coagulation were diagnosed on postmortem. Detectable levels of serum PTHrP support a diagnosis of hypercalcemia of malignancy.     

Lateral thoracotomy and cellophane handing of a congenital portoazygous shunt in a dog

A portoazygous venous shunt was identified in the caudodorsal aspect of the thorax in a young basset hound. During thoracotomy, the anomalous vessel was encircled with sterile cellophane tape. The vein became occluded based on postoperative radiographic examination and improved clinical function five weeks after surgery.     

First detection of canine parvovirus type 2c in pups with haemorrhagic enteritis in Spain

Canine parvovirus type 2 (CPV-2), the aetiological agent of haemorrhagic enteritis in dogs, includes three antigenic variants, types 2a, 2b and 2c. CPV-2c has been detected initially in Italy and subsequently in Vietnam. We report the first identification of this novel antigenic variant in Spain, where it caused an outbreak of fatal enteritis in basset hound pups in association with canine coronavirus type I and type II. We suggest that this new antigenic variant of CPV-2 could spread throughout Europe and that there is a subsequent need to update current CPV vaccines.     

Surgical treatment of right-sided renal lymphoma with invasion of the caudal vena cava

An eight-year-old, male castrated basset hound presenting with a three-month history of lethargy was examined. Diagnostic tests including radiography and ultrasonography showed a right-sided renal mass. A 99mTc diethylenetriamine penta-acetic acid scan demonstrated that this kidney was non-functional. At surgery, invasion of the caudal vena cava was found, and the renal segment of the vena cava and the right kidney were resected. The left renal vein was anastomosed to the more proximal vena cava using a polytetrafluoroethylene graft, and the dog recovered well. Two days postsurgery, the dog suffered an acute episode of aspiration pneumonia and was euthanased. The renal mass was diagnosed as lymphoma on histopathology.     

Stenosis of the thoracolumbar vertebral canal in a basset hound

A three-month-old female basset hound was referred to the Norwegian College of Veterinary Medicine with a history of progressive paresis of the pelvic limbs. Following neurological examination and the study of myelograms, extradural masses causing spinal cord compressions at the T₁₂.₁₃ and T₁₃-L₁ junctions were diagnosed. At necropsy bone-tissue of the vertebral laminae was found to have formed stenoses of the vertebral canal producing compressions of the spinal cord. Irreversible tissue-damage was observed in histological sections prepared from the compressed areas of the spinal cord.     

PALLIATIVE IRRADIATION OF SCOTTISH FOLD OSTEOCHONDRODYSPLASIA

This report describes palliative irradiation as treatment for Scottish Fold osteochondrodysplasia. A 3-year-old female spayed Scottish Fold cat suffering from osteochondrodysplasia was referred to the Veterinary Teaching Hospital, University of Zurich. Based on the breed, history, clinical signs, radiographic findings, and the histologic diagnosis of a biopsy specimen, Scottish Fold osteochondrodysplasia was confirmed. To control the exostoses leading to inflammatory processes and pain, radiotherapy was initiated as palliative treatment. This was successful in relieving the clinical signs within a few weeks. The short- and long-term results after radiotherapy are presented and discussed with a comparable human disease, the plantar heel spur, which also responds well to radiotherapy.     

Intradermal test reactivity to Malassezia pachydermatis in healthy basset hounds and basset hounds with Malassezia dermatitis

Nineteen healthy beagles, eight healthy basset hounds and 17 basset hounds with Malassezia dermatitis were tested intradermally with two extracts of M pachydermatis. One healthy beagle and two affected basset hounds showed wheal and flare reactions 15 minutes after the injection. Delayed reactions, consisting of erythematous macules and plaques, were commonly observed 24 hours after the injection in both the healthy and affected basset hounds, but occurred infrequently in the beagles. At 24 hours the diameters of the lesions in the healthy and affected basset hounds were significantly (P<0.01) greater than those in the healthy beagles, but the diameters in the healthy and affected basset hounds did not vary significantly. Delayed reactions in six of the basset hounds with Malassezia dermatitis were characterised histologically by superficial perivascular and periadnexal infiltrates of neutrophils and lymphocytes.     

Congenital mesoblastic nephroma in a young basset hound dog

An 18‐month‐old male basset hound was presented with vomiting, diarrhoea and depression. Abdominal ultrasonography revealed a mass in the left kidney. An ultrasound‐guided core‐biopsy indicated aggregates of spindle cells, but did not allow a definitive diagnosis. Nephrectomy was performed after a period of six months, when ultrasound examination revealed a slight increase in mass dimensions. Histologically the mass was composed of neoplastic spindle cells forming interlacing fascicles, bundles and whorls, within a loose myxoid to dense collagenous stroma. Immunohistochemically neoplastic cells were positive for vimentin and smooth muscle actin. Based on these findings the tumour was diagnosed as a congenital mesoblastic nephroma, classical variant. After a two‐and‐a‐half‐year follow‐up the dog was clinically healthy, indicating a benign behaviour. To the authors’ knowledge, this report describes the first case of canine congenital mesoblastic nephroma successfully treated surgically, with a reasonable postsurgical follow‐up.     

Growth hormone and Somatomedin. A brief review (author's transl)]

In addition to a direct effect on the metabolic processes of several tissues (table I) growth hormone exerts the functions of a classical trophic hypophyseal hormone by stimulating the synthesis of a secondary hormone. This hormone, Somatomedin, is a growth promoting hormone with cartilage and connective tissues as specific target organ. The activity of somatomedin in plasma changes with the concentration of growth hormone both at the physiological level (constitutional differences in growth rate, fig. 2) and at the pathological level (acromegaly/pituitary dwarfism). The connection between growth hormone and somatomedin at different nutritional conditions is, however, not clearcut. The organ of production of somatomedin, a peptide hormone of ca. 6000 Dalton, is not yet known.     

Cystine calculi I in the dog: an epidemiological retrospective study

During 1970 to 1990, 134 cases of obstructive cystine calculi were diagnosed in Sweden; it was estimated that at least two out of 10,000 male dogs in Sweden had this condition. The disease was found especially in the dachshund, basset hound and Welsh corgi (0–2 to 04 per cent). The study showed that obstructive cystine calculi occur in male dogs of all ages, but not in females or pups. Most cases (53 per cent) were detected at the age of three to five years. Recurrence was common (38 per cent), but was rare in older dogs. Eight dogs which originally had cystine calculi suffered recurrent stones consisting of magnesium ammonium phosphate. Surgery was performed in 40 per cent for the first time (n=122) during the first quarter of the year and in 71 per cent during January to July. Since this condition affects only male dogs after sexual maturity, it was assumed that the formation of cystine calculi involved the sex hormone(s).     

An inherited enchondrodystrophy in the English Pointer dog. A new disease

This report describes the clinical, radiological, pathological and genetic features of an inherited dwarfism in the English Pointer. Gross enlargement of the distal ulnar, radial and tibial growth plates occurred in the first 6 weeks of life and radiographic skeletal abnormalities were present at other sites. The enlargement was due to increase in width of the zone of hypertrophic cartilage, but the columns of chondrocytes were well ordered. By 12 weeks of age an unusual type of degeneration was present beneath the surface of articular cartilage; this developed to widespread, patchy erosion of joint surfaces by 32 weeks. The genetics are compatible with a homozygous recessive mode of inheritance.     

Osteochondrodysplasia in bull terrier littermates

A four-month-old male bull terrier with an abnormal hindquarter gait was found to have changes suggesting nutritional secondary hyperparathyroidism, together with unusual large foci of non-ossified material in both femoral necks and similar smaller foci in metaphyses of several long bones. Abnormal cartilage was found in the one femoral neck examined at autopsy six weeks later, with features suggesting impaired vascular remodelling of cartilage due to failure of chondrocyte maturation. Similar clinical and radiographic abnormalities were found in three littermates (one male, two females), but not the dam. The status of six other littermates and the sire is unknown. The femoral neck lesions had healed in two pups re-examined eight months later, but some limb bones remained abnormal in shape. The abnormalities in affected pups suggested osteochondrodysplasia.     

RETARDATION OF ENDOCHONDRAL OSSIFICATION AT THE DISTAL ULNAR GROWTH PLATE IN DOGS

Bilateral forelimb deformities associated with retained cartilage cores in the distal ulna were diagnosed in 8 immature giant breed dogs. Five of the dogs were autopsied. Histopathological examination of the distal ulnar growth plate revealed a localised central thickening due to the accumulation of hypertrophic chondrocytes which had failed to undergo the usual development to degeneration. Also the intercellular matrix septa of this cartilage were not calcified. Projections of the abnormal cartilage even persisted into the primary spongiosa. These abnormalities in the process of endochondral ossification of the growth plate produced the lesion of retained cartilage core which was responsible for the development of forelimb deformity.     

苏格兰折耳猫骨软骨发育不良的诊疗体会

苏格兰折耳猫骨软骨发育不良也称为苏格兰折耳猫骨营养不良,是影响骨骼生长和关节软骨形成、导致四肢远端和尾部畸形的一种遗传性疾病。一例疑似病例中患畜主要表现为双侧后肢跗关节处肿胀,有疼痛感,爪部、尾部变短、厚,弯曲不灵活。经血常规和影像学检查确诊为苏格兰折耳猫骨软骨发育不良。通过一段时间药物治疗,病情好转,后肢可以着地走路。     

Inherited chondrodysplasia in Texel sheep

CASE HISTORY: A skeletal disease characterised by dwarfism, limb deformity and sometimes sudden death occurred over a period of 5 years in lambs born on a commercial sheep farm in Southland. The disease showed variable expression and occurred in crossbred sheep. A genetic aetiology was supported by the birth of affected lambs over two seasons in a flock of putative carrier and affected sheep transported to Massey University.

CLINICAL FINDINGS: Affected lambs appeared normal at birth but showed evidence of dwarfism, wide-based stance and exercise intolerance as early as 1 week of age. Most died within the first 3 months of life, often after developing bilateral varus deformity of the forelimbs. Some severely-affected lambs died suddenly of respiratory embarrassment, probably due to tracheal collapse. Mildly-affected individuals had a short, blocky stature and some survived to breeding age.

PATHOLOGICAL FINDINGS: Gross and microscopic lesions of variable severity were present in the tracheal, articular, epiphyseal and physeal cartilages. In severe cases, articular cartilage in major joints was eroded from weight-bearing surfaces. The trachea was flaccid, abnormally kinked, and had thickened cartilaginous rings and a narrow lumen. Affected sheep that survived to breeding age eventually developed severe degenerative joint disease. Histologically, chondrocytes were disorganised, surrounded by concentric rings of abnormal fibrillar material, and the matrix often contained focal to coalescing areas of chondrolysis.

DIAGNOSIS: Inherited chondrodysplasia of Texel sheep.

CLINICAL RELEVANCE AND CONCLUSIONS: This chondrodysplasia differs from those previously described in sheep and is considered to be a newly-recognised, recessively-inherited genetic disease of the Texel breed. A defect in the synthesis of glycosaminoglycans in cartilage matrix is suspected. This disease of sheep may provide a suitable model for studying various forms of therapy for human chondrodysplasias.     

Current prevalence of Dirofilaria immitis in dogs, cats and humans from the island of Gran Canaria, Spain

The island of Gran Canaria is a hyperendemic area for canine dirofilariasis. The aim of the present study was to provide data on Dirofilaria immitis in dogs, cats, and humans on this island in 2010. The data confirms the prevalence in the overall canine population (19%), with a considerably higher prevalence (43%) in the autochthonous breed of Canarian Warren hound. The prevalence in the feline population (33%) is higher than that of the canine population, and the existence of specific D. immitis antibodies in the inhabitants of the island of Gran Canaria (12%) is confirmed. In both cats and humans, the prevalence, according to the different climate areas on the island, is related to the prevalence of D. immitis in dogs in the same area, which shows the key epidemiological role played by the canine host with regard to the transmission to other hosts of D. immitis.     

Inbreeding trends and pedigree analysis of Bavarian mountain hounds, Hanoverian hounds and Tyrolean hounds

The objective of this study was to analyse genetic diversity for the three scent-hound breeds Bavarian mountain hound (BMH), Hanoverian hound (HH) and Tyrolean hound (TH) using all available pedigree information from scent-hound kennel clubs for these three breeds throughout Europe. The pedigree data of the BMH and the HH date back to 1912 and 1894, respectively. Pedigree data of the TH were available from the 1960s onwards. The reference populations included all BMH (n = 3231), HH (n = 1371) and TH (n = 1167) dogs registered between 1992 and 2004. Average generation intervals were 5.3 years for the BMH and 5.0 years for the HH and TH. Average inbreeding coefficients for the reference populations were 4.5%, 6.8% and 9.5% for the BMH, HH and TH. The effective numbers of founders, ancestors and founder genomes were lowest for the TH and highest for the BMH. The effective numbers of founder genomes were 10.9, 5.6 and 4.3 for the BMH, HH and TH. Effective population size was largest for the BMH with 72.7 effective breeding animals, followed by the HH with 50.9 and TH with 26.5. The most important ten ancestors had genetic contributions to the reference populations of 54.4%, 65.2% and 77.9% in the BMH, HH and TH. The results of our study indicate the need for careful breed management in these highly specialized hound breeds to maintain genetic diversity. European stud books should be established for these dog breeds in order to avoid inbreeding due to missing pedigree records.     

Delayed growth in two German shepherd dog littermates with normal serum concentrations of growth hormone, thyroxine, and cortisol

Four German Shepherd Dogs from a litter of 10 were evaluated because of postnatal onset of proportionate growth stunting that clinically resembled well-documented hypopituitary dwarfism in that breed. Although 2 pups had histologic evidence of hypopituitarism, the remaining 2 pups had normal serum growth hormone concentration and adrenocorticotropin secretory capability, and normal adrenal function test and thyroid function study results. Furthermore, the initially stunted German Shepherd Dogs grew at a steady rate until at 1 year, body weight and shoulder height approximated normal measurements. Seemingly, delayed growth in these pups may represent one end of a clinical spectrum associated with hypopituitarism in German Shepherd Dogs.