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Clinical and Oral Manifestations in a Patient with Lenz-Majewski Syndrome: A Rare Case Report. [PDF]
BMC Oral HealthBayram M, Akgöl BB, Çetin E, Ceylan G.
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Metabolic programming in tooth development: a regulatory network from energy substrates to signaling instructions. [PDF]
Front Cell Dev BiolCao X, Gao Y, Liu W, Sun X.
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Tmem2 Deficiency Leads to Enamel Hypoplasia and Soft Enamel in Mouse
Journal of Dental Research, 2023Teeth consist of 3 mineralized tissues: enamel, dentin, and cementum. Tooth malformation, the most common craniofacial anomaly, arises from complex genetic and environmental factors affecting enamel structure, size, shape, and tooth eruption. Hyaluronic acid (HA), a primary extracellular matrix component, contributes to structural and physiological ...
P. Nag +10 more
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Clinical Genetics, 1971
An extensive family with a total of forty–one individuals who are either affected or reputed to be affected with hereditary hypoplasia of the enamel is presented. The distribution of patients, which spans four generations in this pedigree, appears to be consistent with X–linked dominant inheritance of the disorder.
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An extensive family with a total of forty–one individuals who are either affected or reputed to be affected with hereditary hypoplasia of the enamel is presented. The distribution of patients, which spans four generations in this pedigree, appears to be consistent with X–linked dominant inheritance of the disorder.
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Enamel Hypoplasia – A Clinical Review
Dental Journal of Indira Gandhi Institute of Medical Sciences, 2023As a result of congenital and developmental systemic diseases, errors in the growing enamel organ result in enamel abnormalities such as enamel hypoplasia or opacities. The great occurrence of these flaws shows how susceptible teeth are to alterations in the prenatal and postnatal environment.
Rashmi Rokade +5 more
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The etiology of enamel hypoplasia: A unifying concept
The Journal of Pediatrics, 1981In a study of children with chronic disorders of calcium and phosphate homeostasis, enamel hypoplasia was found in hereditary vitamin D-dependency rickets and in hypoparathyroidism, conditions characterized by hypocalcemia, and was not found in X-linked hypophosphatemic rickets, a condition in which the plasma calcium concentration is normal.
G, Nikiforuk, D, Fraser
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Enamel hypoplasia in a Canadian historic sample
American Journal of Human Biology, 1999Analyses of historical skeletal samples provide useful comparisons of the prevalence of skeletal indicators of stress to documentary information on health, diet, and socioeconomic status. A sample of the permanent dentitions of 253 adults from the St.
Shelley R., Saunders, Anne, Keenleyside
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Early hominid enamel hypoplasia
American Journal of Physical Anthropology, 1978AbstractEnamel hypoplasia in the South African Plio‐Pleistocene fossil hominid sample is examined. The Swartkrans hominids are shown to have a higher incidence of hypoplasia than the Sterkfontein hominids. Within the Swartkrans sample, individuals with hypoplasia of the first upper molar have lower‐than‐expected ages of death.
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Pitted enamel hypoplasia in tuberous sclerosis
Clinical Genetics, 1992Thirty patients with tuberous sclerosis (from 29 different families) were examined for evidence of macroscopically visible pitted enamel hypoplasia. Of 23 patients with permanent teeth, 11 (48%) showed multiple enamel pits (mean 4.6 pits, range 3–9), but none were seen in six patients with deciduous teeth.
J R, Sampson +3 more
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