Results 191 to 200 of about 34,364 (292)
ABSTRACT Background Treacher Collins Syndrome (TCS) is an uncommon congenital disease of the craniofacial complex. While there are ‘classic’ facial manifestations of TCS, they present with a wide range of variability. Face2Gene (F2G) is a deep‐learning algorithm that can provide differential diagnoses of syndromes via analysis of 2‐dimensional facial ...
Jie Han Timothy Sng +2 more
wiley +1 more source
<i>SRSF1</i> haploinsufficiency drives the neurodevelopmental phenotype of the 17q22 deletion syndrome. [PDF]
Wu Y +5 more
europepmc +1 more source
ABSTRACT Objective Unilateral craniofacial microsomia (UCM) presents varying unilateral deficiencies of the temporomandibular joint, mandibular ramus, masticatory muscles, and adjacent soft tissues and ear. Reduced mandibular and maxillary dimensions may decrease upper airway volume and may increase the risk of sleep‐disordered breathing (SDB).
Akila Aiyar +3 more
wiley +1 more source
Prevalence and maternal-child clinical and socioeconomic factors associated with congenital anomalies in a Mexican hospital-based setting. [PDF]
Salinas-Torres VM, Salinas-Torres RÁ.
europepmc +1 more source
Quality of Online Information Relating to Cleft Lip and Palate: A Scoping Review
ABSTRACT Individuals with orofacial clefts experience a substantial lifetime burden of medical, surgical and dental care, often requiring complex treatment decisions. This scoping review aimed to collate and critically assess the available literature regarding the quality and readability of online cleft‐related information.
Emilija D. Jensen +6 more
wiley +1 more source
Phenotypic Spectrum and Chromosomal Discordance in Alobar Holoprosencephaly: A Comparative Case Series from a Tertiary Referral Center. [PDF]
Caropeboka MFA +4 more
europepmc +1 more source
ABSTRACT Background R‐Loops are three‐stranded DNA/RNA hybrids implicated in immune responses. Their role in mesenchymal stem cell differentiation, particularly in dental pulp regeneration under inflammation, remains unclear. Methods Rat pulpo‐dentinal complex (PDC) injury models and LPS‐stimulated human dental pulp stem cells (hDPSCs) were used.
Yun Yang +5 more
wiley +1 more source
First Case Report of Agnathia-Otocephaly Complex Reported in Niger. [PDF]
Diaouga HS +3 more
europepmc +1 more source
ABSTRACT Introduction The aim of this study was to obtain the views of oral surgeons (OS) and oral and maxillofacial surgeons (OMFS) in the United Kingdom on labial frenectomies regarding their indication, timing and preferred surgical techniques. Materials and Methods This was a cross‐sectional, questionnaire‐based study.
Dawn Anne Yip Xinying +3 more
wiley +1 more source
Patient-derived AMOTL1 mutations lead to defective cell migration and tissue development. [PDF]
Luo J +11 more
europepmc +1 more source

