hypoplasia in English

noun

abnormal or incomplete development of an organ or tissue (Medicine)

Use "hypoplasia" in a sentence

1. Bull Infertility Congenital infertility Testicular hypoplasia

2. Hypoplasia is a see also of Aplasia

3. Bolten frequently treats Facial Reconstruction, Dentofacial Anomalies, and Mandibular Hypoplasia

4. Syndrome of camptodactyly, multiple Ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition.

5. So Aplasia means “no development”, and “hypo” means “under” so hypoplasia is “under formation”

6. Syndrome of camptodactyly, Ankyloses, facial anomalies, and pulmonary hypoplasia (Pena-Shokeir syndrome): obstetric and ultrasound aspects

7. Achondroplasia is the most common short-stature skeletal dysplasia, additionally marked by rhizomelia, macrocephaly, midface hypoplasia, and normal cognition

8. Objective To identify factors predicting performance outcomes following cochlear implantation in patients with cochlear nerve Aplasia or hypoplasia

9. Twenty-one (20%) Aplasias of the left sinus, 41 (39%) hypoplasia of the left sinus, 33 (31%) symmetric, 6 (6%) hypoplasia of the right sinus, and 4 (4%) Aplasias of the right sinus cases were determined in the asymmetry in sizes of transverse sinuses.

10. Congenital muscular dystrophy with Adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD Neuromuscul Disord

11. As nouns the difference between hypoplasia and Aplasia is that hypoplasia is underdevelopment or incomplete development of a tissue or organ, especially when caused by an inadequate or below-normal number of cells while Aplasia is (pathology) a condition marked by the incomplete development, or absence, of an organ or tissue.

12. Ureteral Aplasia (agenesis) is the lack of formation of a recognizable ureter, and hypoplasia is the presence of a notably small-diameter ureter

13. Cyclotocephaly is a very rare malformative lethal condition which associates otocephaly (extreme hypoplasia of the mandibular arch with agnathia) and cyclopy with proboscis.

14. Cerebellar abiotrophy in horses was originally thought to be a form of cerebellar hypoplasia (CH) and was described as such in older research literature.

15. Furthermore malformations as amastia, athelia, polymastia, polythelia, breast hypoplasia and breast hypertrophy, breast asymmetria, tuberous breast deformity, funnel chest, Poland’s syndrome and inverted nipples are described.

16. We report a case of pulmonary hypoplasia associated with renal agenesia diagnosed in a 46-year-old woman admitted to hospital because of a viral pleuro-pericarditis.

17. In the newborn of an 18 year old primigravida “caudal regression” was observed with agenesia of the axial skeleton below Th 9, atresia of the rectum and hypoplasia of both kidneys.

18. Presented is a case of congenital agenesis of the M3 and prenatally formed enamel and coronal dentine hypoplasia of the M1 in the lower jaw of a roe buck, aged about 18 months.

19. Several factors (midfacial hypoplasia, muscular hypotonia, narrowing of the foramen magnum) related to achondroplasia contribute to the fact that achondroplastic children and adolescents have an increased risk for SRD and chronic respiratory failure.

20. Other candidates for the surgery include babies born with a microphallus, people with Müllerian agenesis resulting in vaginal hypoplasia, transgender or transsexual women, and women who have had a vaginectomy after malignancy or trauma.

21. Caudal regression syndrome (CRS), also known as Caudal regression sequence, Caudal dysplasia, Caudal aplasia, femoral hypoplasia, phocomelic diabetic embryopathy, or sacral agenesis, is a spectrum of anomalies involving the Caudal end of the trunk

22. Choanal Atresia may be associated with various other anomalies, CHARGE syndrome is the most common of these and consists of coloboma, heart disease, Atresia choanae, growth, and mental retardation, genital hypoplasia, and ear anomalies

23. The present report treats a female stillborn human Anencephalous fetus with the craniorrhachischisis, cleft palate, left-sided congenital diaphragmatic hernia, hypoplasia of lungs, imperforate vagina and anus, absent left kidney and sternal muscle on the left side

24. Since this is slightly shorter than older descriptions, it may impact the diagnosis of women with vaginal agenesis or hypoplasia who may unnecessarily be encouraged to undergo treatment to increase the size of the vagina.

25. The fetal Akinesia deformation sequence (FADS) refers to a clinically and genetically heterogeneous constellation of features including fetal Akinesia, intrauterine growth retardation, arthrogryposis, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism (Vogt et al., 2009).

26. Diseases associated with Cask include Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia and Fg Syndrome 4.Among its related pathways are Neuroscience and Neurotransmitter Release Cycle.Gene Ontology (GO) annotations related to this gene include transferase activity, …

27. There were hypoplasia of amniotic cavity, abnormal connection of amnion to the embryo body, disturbed topographic position of the embryo in the embryo membrane, lack of internal organ rudiments, hypoplasiy of the allantoid stalk and of chorion frondosum.

28. Since similar changes are also observed in kidney hypoplasia, bilateral advanced cystic kidney, and urethraatresia, the question was raised whether dysplasia renofacialis should be regarded as a syndrom in its own right; the following, some-what far-reaching, definition was proposed: A case should only be described as dysplasia renofacialis if in the presence of a so-called “functional renal agenesia” (no secretion of urine into the amniotic fluid), typical facial changes are observed which usually go together with a hypoplasia of the lungs.

29. Cretin Congenital hypothyroidism Endocrinology A person with defective thyroxine or thyroglobulin synthesis Etiology Goiter, iodine deficiency in the mother while pregnant; thyroid gland defects–aplasia, hypoplasia or dysgenesis Clinical Cold intolerance, serosal effusions, myxedema, ↓ metabolic rate, ↑ cholesterol, profound mental retardation–hypothyroid idiocy, ↓ growth.

30. 20 to 40% of Amblosis cases, and the risk thereof doubles in cases of multiple fetation and abnormal alvus development9 and is the cause of 20-50% of all premature delivery cases, mother’s and perinatal mortality, fetus’s lung hypoplasia, prolapse of funis, deformity of fetus, and postpartum endometritis.12

31. Cask-related intellectual disability is a disorder of brain development that has two main forms: microcephaly with pontine and cerebellar hypoplasia (MICPCH), and X-linked intellectual disability (XL-ID) with or without nystagmus.Within each of these forms, males typically have more severe signs and symptoms than do females; the more severe MICPCH mostly affects females, likely because only a

32. Not counting the 17 per cent of cases with monstrous deformities which were found in kidney agenesia, the following clinical and pathologic-anatomical findings were obtained: agenesia of the kidneys and ureters in 100 per cent; typical facial dysplasia (Potter) in 82 per cent; deformities of the internal male and female genital organs in 80 to 100 per cent; microcystis in 74 per cent; hypoplasia of the lungs in 70 per cent; club foot in 31 per cent, deformities of the spine in 15 per cent; analatresia in 12.5 per cent; malformation of the external genital organs in 12.5 per cent; contracted joints in 11.5 per cent of the cases.