Sentences with phrase «hypoplasia in»

Examples of the latter might include: choroidal hypoplasia in breeds not previously identified as having Collie Eye Anomaly, optic nerve colobomas, microphthalmia, multi-focal retinopathy in breeds not yet recognized as having CMR mutations, etc..

Old English Sheepdog, Gordon setter, Scottish terrier, Staffordshire terrier, spinone iltaliano and Finnish hounds occasionally suffer from a different genetic defect that produces symptoms quite similar to cerebellar hypoplasia in kittens.

All Aussies affected with CEA will exhibit choroidal hypoplasia in both eyes.

I couldn't find any references to cerebellar hypoplasia in pugs on an initial literature search but did find reference to this problem in a couple of other breeds (Gordon setters and Kerry blue terriers).

This means that regular vaccination will prevent cerebellar hypoplasia in kittens.

The distemper virus can cause cerebellar hypoplasia in a kitten, a condition in which the cerebellum doesn't develop properly.

Not exact matches

In addition, if you are a healthcare provider working with a woman with diabetes, PCOS, hypoplasia or other conditions that impact her fertility, it is important to talk to her about the potential impact on her ability to breastfeed.

However, like with diabetes and PCOS, assisted fertility and hormonal support to conceive babies is leading to an increase in the number of cases of babies born to mothers with hypoplasia.

Not a lot is known about the causes of mammary hypoplasia, but there is likely a genetic link (women who have it often say that no one in their family was able to breastfeed).

Research on IGT (also called breast hypoplasia and tuberous breasts) and its effect on lactation is almost nonexistent, with the most widely quoted study cobbled together in 2000 by enterprising nurses and lactation consultants who assembled 33 breast - feeding women with breast characteristics that they suspected were linked to low milk production.

Some mothers with hypoplasia / IGT report luteal phase defect, which is a cyclical occurrence of lower - than - normal progesterone, even in the presence of ovulation.

Called tubular (or tuberous) breast deformity in the plastic surgery literature, hypoplasia of the mammary gland (also called insufficient glandular tissue or IGT) was previously thought to be a simple issue of cosmetics — corrections addressed the appearance of a woman's breasts, with little regard for their function.

Obstetricians, midwives, and perinatal nurses, pediatricians, and lactation consultants who have contact with mothers in the immediate post partum period should be alert for and suspicious of mothers who appear to have breast hypoplasia and widely spaced breasts.

The majority of the women with some degree of hypoplasia and an intramammary distance of 1.5 inches or more produced 50 % or less of the milk necessary to sustain normal infant growth in the first week postpartum.

Many lactation consultants only encounter mothers with breast hypoplasia after discharge when they are referred with their infants in various states of nutritional compromise.

Lactation consultants can be instrumental in orienting all of the health professionals who have contact with pregnant and newly delivered women to this condition and the related implications of breast hypoplasia.

Mothers who appear to have breast hypoplasia can and should be identified in the prenatal or immediate post partum period.

Called «breast hypoplasia» or» insufficient glandular tissue,» in this situation, there are not enough milk - making glands to produce 100 % of the milk a baby needs.

I want to thank you for your question, Hypoplasia Breast Syndrome is something that a lot of medical professional haven't really familiarized themselves with although it is estimated that it has been there for one in a thousand moms deal with some form of the syndrome.

I just stumbled upon the diagnosis of hypoplasia and was wondering if this is in fact my issue?

All of the patients were found to have significant fovea hypoplasia (an underdevelopment of the macula, the center of the retina), a characteristic not commonly seen in other achromatopsia patients.

Scientists at the Virginia Tech Carilion Research Institute (VTCRI) have revealed the pathology of cells and structures stricken by optic nerve hypoplasia, a leading cause of childhood blindness in developed nations.

Optic nerve hypoplasia is closely related to optic nerve atrophy, in which the optic nerve develops normally initially, but later degenerates as its cells die off.

The teen had cavities, dental crowding, and hypoplasia, a line indicating that enamel growth was halted at some point in childhood, probably because of malnutrition or disease.

Following a Forward Genetics approach, Fleming researchers identified a novel neurological mouse model caused by a functional mutation in the Slc25a46 gene, a new pathogenic target in a wide spectrum of human neurological diseases, including optic atrophy, Charcot - Marie - Tooth type 2, Leigh syndrome, progressive myoclonic ataxia and lethal congenital pontocerebellar hypoplasia.

Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene

Optic nerve hypoplasia with the double - ring sign, increased cup - disc ratio, attenuated blood vessels, gross pigment mottling, and chorioretinal scar in the macular region.

Biallelic mutations in the 3» exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing.

Loss of function mutations in human Oligophrenin1 (OPHN1) gene are responsible for syndromic intellectual disability (ID) associated with cerebellar hypoplasia and cerebral ventricles enlargement.

However, it is fairly common to see Cerebellar Hypoplasia (an under - developed brain portion) in response to a Parvo Virus (feline distemper) infection in the mother cat during pregnancy.

In clinical safety studies, some dogs that received 3 or 5 times the maximum recommended dosage of Iverhart Max for 6 months presented with testicular hypoplasia.

Crowns are also used as a second layer of defense in cases where protective enamel is not present due to wear, or congenital disease causing part of the enamel not to form (enamel hypoplasia).

Potential etiologies for EPI in younger cats could include pancreatic acinar atrophy, pancreatic hypoplasia or aplasia, and Eurytrema procyonis infestation.

If a dog has only choroidal hypoplasia sometimes the natural pigment in the back of the eye hides its presence.

Veterinary Record 153: 107 - 112 Rusbridge C and Knowler SP, 2004 Inheritance of Occipital Bone Hypoplasia (Chiari type I malformation) in Cavalier King Charles spaniels.

References Rusbridge C and Knowler SP, 2003 Hereditary aspects of occipital bone hypoplasia and syringomyelia (Chiari type I malformation) in cavalier King Charles spaniels.

Progressive retinal atrophy (PRA), glaucoma, enamel hypoplasia, Legg - Perthe's disease, leg bone breaks in young dogs, patellar luxation, autoimmune diseases, hemangiosarcoma, congenital megaesophagus, progressive periodontal disease, portosystemic shunts, masticatory myopathy, vitreous degeneration, cataracts, lens luxation, color dilution alopecia, and epilepsy.

The resulting kittens are likely to be born with cerebellar hypoplasia, a disorder of the brain, and therefore be uncoordinated in their movement and suffer from head tremors.

(The eye anomaly «merle» can be confused with choroidal hypoplasia, primarily in dogs from merle to merle breeding and whose coat color is whiter than their littermates.

No treatment can resolve the damage in a kitten with cerebellar hypoplasia.

Vaccination, at least with a live vaccine, should be avoided during pregnancy as cerebellar hypoplasia (see above) can result in the kittens.

These puppies are not subject to tracheal hypoplasia often seen in the English bulldog.

Border Collie breeders are usually very proactive in testing for the genetic diseases Collie Eye Anomaly / Choroidal Hypoplasia, Neuronal Ceroid Lipofuscinosis and Trapped Neutrophil Syndrome, but you should check with your breeder before buying a Border Collie on the status of their dogs for genetic diseases.

The female cat either infected in pregnancy or vaccinated with live virus during pregnancy can produce kittens with a specific birth defect called «Cerebellar hypoplasia» a brain malformation that leads to tremoring and wobbling particularly when the cat is attempting a specific task (the so - called «intention tremor.»)

All dogs with CEA have bilateral choroidal hypoplasia (CH), also called chorioretinal dysplasia, a thinning of the vascular tissue in the back of the eye which does not significantly impair vision.

Choroidal hypoplasia (CH,) the most common CEA defect, is present in all affected dogs.

Most the affected offspring in these litters had choroidal hypoplasia.

In particular, she focuses upon Cerebellar Hypoplasia (aka Wobbly Cat Syndrome).

Testicular hypoplasia was seen in dogs receiving 50 mg / kg.

Testicular hypoplasia was seen in dogs treated for 1 year at 12.5 times the maximum daily dose.