turner's hypoplasia in a sentence

• adrenal hypoplasia    X-linked adrenal hypoplasia congenita is caused by mutations in the NR0B1 gene. Adrenal hypoplasia and growth hormone deficiency are associated endocrine consequences of Ritscher-Schinzel ...
• adrenal hypoplasia congenita    X-linked adrenal hypoplasia congenita is caused by mutations in the NR0B1 gene. This deletion results in a condition called adrenal hypoplasia congenita with complex glycerol kinase defici...
• agenesis and hypoplasia of the lung    Agenesis and hypoplasia of the lung
• bilateral hypoplasia    Types of breast asymmetry include bilateral asymmetric hypertrophy, unilateral hypertrophy with normal contralateral breast, unilateral hypertrophy with amastia or hypoplasia of the contra...
• breast hypoplasia    Insufficient glandular tissue of the breasts, or breast hypoplasia, caused by a lack of normal mammary gland growth and maturation during puberty and / or pregnancy, is another cause of la...
• cartilage hair syndrome hypoplasia    On his foundation's Web site, Barty says : " The name of my condition is Cartilage Hair Syndrome Hypoplasia, but you can just call me Billy ." Actor Verne Troyer is affected with this form...
• cartilage-hair hypoplasia    Cartilage - hair hypoplasia
• cerebellar hypoplasia    Cerebellar hypoplasia causes jerky movements, tremors and generally uncoordinated motion. Cerebellar hypoplasia is particularly common in cats and has similar symptoms. Patients have cereb...
• cerebral hypoplasia    Mutations in the RELN gene appear in the autosomal form of lissencephaly with cerebral hypoplasia, where patients show developmental delay, hypotonia, ataxia and seizures, symptoms which c...
• congenital adrenal hypoplasia    This protein also functions as an anti-testis gene by acting antagonistically to SRY . Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hyp...
• congenital hypoplasia    Some researchers have suggested that the underlying problem of this disorder could be congenital hypoplasia or agenesis of the cranial nerve nuclei.
• dental enamel hypoplasia    Studies of dental enamel hypoplasia are used to study child health. Lack of association between celiac disease and dental enamel hypoplasia in a case-control study from an Italian central ...
• dental hypoplasia    Dental hypoplasias provide an indicator of health status during the time in childhood when the enamel of the tooth crown is being formed.
• dermal hypoplasia    The differential diagnosis of focal dermal hypoplasia ( Goltz ) syndrome includes autosomal recessive Setleis syndrome due to TWIST2 gene mutations. The differential diagnosis of Setleis s...
• enamel hypoplasia    Studies of dental enamel hypoplasia are used to study child health. This type of deformity is also thought to be caused by enamel hypoplasia. With relations to dentistry, a deficiency in V...
• femoral hypoplasia    A corresponding condition affecting the hind legs is called Femoral Hypoplasia and has only been reported three times in cats.
• focal dermal hypoplasia    The differential diagnosis of focal dermal hypoplasia ( Goltz ) syndrome includes autosomal recessive Setleis syndrome due to TWIST2 gene mutations. The differential diagnosis of Setleis s...
• foveal hypoplasia    Thus, some aniridic individuals are only missing a relatively small amount of iris, do not have foveal hypoplasia, and retain relatively normal vision. The aniridic probands showed typical...
• hypoplasia    Maxillary hypoplasia ( midfacial retrusion ) was significant in many patients. Studies of dental enamel hypoplasia are used to study child health. Cerebellar hypoplasia causes jerky moveme...
• hypoplasia of the corpus callosum    Hypoplasia of the corpus callosum is also a common finding. Mutations in the WDR62 gene cause of a wide spectrum of severe cerebral cortical malformations including microcephaly, pachygyri...
• hypoplasia of the sacrum    "' Caudal regression syndrome "'or "'sacral agenesis "'( or hypoplasia of the sacrum ) is a congenital disorder in which there is abnormal fetal development of the lower spine the caudal ...
• hypoplasia of the uterus    Endocrinopathy manifests as amenorrhea and hypoplasia of the uterus.
• leydig cell hypoplasia    Leydig cell hypoplasia does not occur in biological females as they do not have either Leydig cells or testicles. Leydig cell hypoplasia is caused by genetic mutations in " LHCGR ", a gene...
• mandibular hypoplasia    It is also sometimes called " Mandibular hypoplasia ". A mutation in the GSC gene causes short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities ( SAMS ). ...
• maxillary hypoplasia    Maxillary hypoplasia ( midfacial retrusion ) was significant in many patients. These are : wrinkly, loose skin over the face, abdomen, and extremites ( hands, feet ) on the fractures; maxi...