Results 31 to 40 of about 40,078 (160)

Soft tissue thickness of face profile conditioning by dento-skeletal anomalies [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2011
Introduction. Orthodontic treatment of dento-skeletal anomalies is generally based on the correction of teeth and jaws relationship, while it is expected that soft facial tissue spontaneously adapts to therapeutically achieved relationship and to ...
Tanić Tatjana, Blažej Zorica, Mitić Vladimir   +2 more
doaj   +1 more source

Associations between 44 nonmetric permanent dental traits or anomalies with skeletal sagittal malocclusions and sex, besides correlations across the variations or abnormalities

BMC Oral Health, 2022
Introduction Nonmetric dental traits and the shape, size, or number of dental anomalies are essential to various dental fields such as orthodontics, dental anatomy, anthropology, pathology, and forensic dentistry.
Negin Ashoori, Fataneh Ghorbanyjavadpour, Vahid Rakhshan   +2 more
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Skeletal Anomalies in Juveniles of Siberian Grayling Thymallus arcticus (Pallas, 1776) from the Mana River (Middle Yenisei River System) under Artificial and Natural Reproduction [PDF]

Журнал Сибирского федерального университета: Серия Биология, 2017
The paper contains data on diversity and frequency of occurrence of skeletal anomalies in larvae and juveniles of Siberian grayling from the Mana river (Middle Yenisei River system) grown both in the temporary fish-breeding farm and under natural ...
Nikita O. Yablokov
doaj  

Specific heterozygous variants in MGP lead to endoplasmic reticulum stress and cause spondyloepiphyseal dysplasia

Nature Communications, 2023
Matrix Gla protein (MGP) is a vitamin K-dependent post-translationally modified protein, highly expressed in vascular and cartilaginous tissues. It is a potent inhibitor of extracellular matrix mineralization.
Ophélie Gourgas, Gabrielle Lemire, Alison J. Eaton, Sultanah Alshahrani, Angela L. Duker, Jingjing Li, Ricki S. Carroll, Stuart Mackenzie, Sarah M. Nikkel, Care4Rare Canada Consortium, Michael B. Bober, Kym M. Boycott, Monzur Murshed   +12 more
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An orthodontic perspective on Larsen syndrome

BMC Oral Health, 2021
Background Larsen syndrome (LS) is a rare disorder of osteochondrodysplasia. In addition to large-joint dislocations, craniofacial anomalies are typical characteristics.
Madoka Yasunaga, Hiroyuki Ishikawa, Kenichi Yanagita, Sachio Tamaoki   +3 more
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Hydrolethalus Syndrome: A Case of a Rare Congenital Disorder

Diagnostics
This is a fatal case of multiple complicated congenital anomalies displaying several symptoms consistent with hydrolethalus syndrome. The newborn’s phenotype is characterized by a combination of serious anatomical abnormalities such as open-book cerebral
Valerica Belengeanu, Diana Marian, Horia Ademir Stana, Carolina Cojocariu, Cristina Popescu, Ioana Elena Lile   +5 more
doaj   +1 more source

Bilateral Femoral Duplication and Fibular Agenesis Associated with Bilateral Lower Limb Ectrodactyly: A Rare Case Report

International Journal of Anatomy Radiology and Surgery, 2018
Limb deficiency disorders are rare, aetiologically heterogeneous skeletal dysplasias, they may occur as an isolated anomaly or as a part of syndrome.
Chetan M, Santosh Reddy Patil, Bharathi M, Vamshi Krishna, Ravi Garg   +4 more
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Cadaveric kidney transplantation in an ESRD patient with Klippel–Feil syndrome—A case report

Clinical Case Reports, 2023
Klippel–Feil syndrome (KFS) is a congenital skeletal disorder with classic clinical triad consisting of short neck, low hairline, and limitation of neck movement.
Hossein Dialameh, Farshad Namdari, Farhad Etezadi, Seyed Hassan Inanloo, Seyed Hamid Mousavi, Hormat Rahimzadeh, Mohammad Javad Nazarpour   +6 more
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Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 cases

Frontiers in Genetics
This study assessed the diagnostic effectiveness of trio-WES compared to CMA in fetuses with ultrasound anomalies and explored optimal prenatal testing strategies. A retrospective review included 454 fetuses who underwent trio-WES and/or CMA between 2020
Dongyi Yu, Dongyi Yu, Dongyi Yu, Dairong Feng, Dairong Feng, Dairong Feng, Jiangbo Qu, Jiangbo Qu, Jiangbo Qu, Lei Nie, Qian Liu, Lu Gao, Lu Gao, Lu Gao, Wenzhen An, Na Liu, Na Liu, Na Liu, Yuying Fang, Yuying Fang, Yuying Fang   +20 more
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STAT3-Mediated Transcriptional Regulation of Osteopontin in STAT3 Loss-of-Function Related Hyper IgE Syndrome

Frontiers in Immunology, 2018
BackgroundHyper-IgE syndrome (HIES) caused by loss-of-function (LOF) mutations in STAT3 gene (STAT3 LOF HIES) is associated with dental and facial abnormalities in addition to immunological defects.
Shubham Goel, Smrity Sahu, Ranjana W. Minz, Surjit Singh, Deepti Suri, Young M. Oh, Amit Rawat, Shobha Sehgal, Biman Saikia   +8 more
doaj   +1 more source