Results 61 to 70 of about 84,661 (166)
Enamel defects and Lyonization in focal dermal hypoplasia
We report a pattern of enamel hypoplasia in focal dermal hypoplasia similar to that found in females with X-linked amelogenesis imperfecta. Three cases of focal dermal hypoplasia are described, with specific focus on the oral and dental features.
Aldred, M.J. +3 more
core +1 more source
ABSTRACT Interglobular dentin (IGD) has been used as a biomarker for vitamin D deficiency (VDD) in past populations. However, an evidence‐based threshold for the levels of serum vitamin D associated with IGD occurrence has not been established. Here, we explore the association between perinatal serum vitamin D levels, presence of IGD, and biological ...
Anne Marie Sohler‐Snoddy +6 more
wiley +1 more source
Result of Study on a Kindred with Hereditary Enamel Hypoplasia [PDF]
A nine month old female was found to have hereditary enamel hypoplasia at ABCC clinic, Nagasaki, in 1953. Subsequently, eleven out of 34 members examined in this kindred were found to have enamel hypoplasia in three generations.
錬石, 昇太郎
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Dentofacial Characteristics in Patients With Epidermolysis Bullosa—A Cross‐Sectional Study
ABSTRACT Objectives Epidermolysis bullosa (EB) is a rare genetic disease characterized by skin and mucosal fragility caused by pathogenic variants in structural protein genes. Malocclusions have been previously described in patients with EB, mainly in case reports, with no cohort studies characterizing dentofacial characteristics across all EB types ...
Sebastián Véliz +3 more
wiley +1 more source
Enamel hypoplasia in a medieval population from Slaboszewo [PDF]
ENAMEL HYPOPLASIA IN A MEDIEVAL POPULATION FROM SLABOSZEWO. Enamel hypoplasia in 68 individuals from a medieval cemetery of Slaboszewo (North-Western Poland) was analysed. Individual ages at defect development were assessed.
Krem, Marta, Piontek, Janusz
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Occurrence of epidermolysis bullosa along with Amelogenesis imperfecta in female patient of India
Epidermolysis bullosa (EB) is an inherited disorder, which is characteristically presented as skin blisters developing in response to minor injury. Junctional variety of EB is also associated with enamel hypoplasia.
A P Javed +5 more
doaj +1 more source
OBJECTIVES:The study tried to determine if malnutrition (underweight, stunting, wasting, overweight) and enamel defects (enamel hypoplasia, hypomineralized second molar, amelogenesis imperfecta, fluorosis) were associated with early childhood caries (ECC)
Morenike Oluwatoyin Folayan +5 more
doaj +1 more source
The role of Rho GTPases in facial morphogenesis
The role of small GTPases, RHOA, RAC1, and CDC42 and pathway mediators is reviewed in the context of embryonic facial development. Lip fusion requires cytoskeletal remodeling during morphogenesis of the facial processes and during lip fusion. Fnm, frontonasal mass; lnp, lateral nasal process; mnp, medial nasal process; mxp, maxillary process; np, nasal
Isra Ibrahim, Joy M. Richman
wiley +1 more source
Hyperemesis gravidarum and oral health: A scoping review
Abstract Background Hyperemesis gravidarum (HG) is a severe form of nausea and vomiting in pregnancy (NVP), associated with dehydration, nutritional deficiencies, and systemic complications. Although recurrent vomiting, altered dietary patterns, and medication effects might plausibly affect oral health, this relationship has not been comprehensively ...
Niamh Coffey +4 more
wiley +1 more source
Enamel hypoplasia or amelogenesis imperfecta - a restorative approach [PDF]
Genetic or acquired disturbances may lead to the development of alterations on enamel structure, compromising tooth esthetics and function. This short communication aims to briefly discuss the possibility of employment of several treatment options ...
Adérito Soares da Mota +4 more
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