Results 61 to 70 of about 117,613 (171)
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities
Background: A long list of syndromic entities can be diagnosed immediately through scrutinizing the clinical phenotype of the craniofacial features. The latter should be assisted via proper radiological interpretations.
Ali Al Kaissi +11 more
doaj +1 more source
Background and Objectives: Positional plagiocephaly is one of the most common skull deformities that ultimately lead to the asymmetry of the head and face in different ranges.
Esmaeil Chahaki +3 more
doaj
Equity and Respect in Maternal and Infant Healthcare—A Report From the 2025 Venice Forum
ABSTRACT Aim To examine equity and respectful care for women and infants from five perspectives: the global context; economic issues; healthcare systems; legal and policy issues; opportunities to benefit from biomedical research. Methods Narrative review.
Mark Hanson +15 more
wiley +1 more source
Positional cranial deformities are relatively common conditions, characterized by asymmetry and changes in skull shape. Although three-dimensional (3D) scanning is the gold standard for diagnosing such deformities, it requires expensive laser scanners ...
Cecilia A. Callejas Pastor +5 more
doaj +1 more source
Positional posterior plagiocephaly: a single-center review [PDF]
OBJECTIVEThe authors sought to assess the prevalence and severity of positional posterior plagiocephaly (PPP) in the pediatric population at a tertiary care center.METHODSThe authors conducted a retrospective review of 1429 consecutive patients aged 2 months to 18 years who presented with head trauma and a negative CT scan in 2018.
Ranbir, Ahluwalia +6 more
openaire +2 more sources
Positional Plagiocephaly: Definition, Diagnosis and Treatment
Positional plagiocephaly (PP) is a non-synostotic cranial asymmetry that has risen in prevalence in the supine-sleep era. This review synthesizes current evidence on definition, differential diagnosis, assessment, and treatment, emphasizing practical ...
Ozan Işık, Süleyman Akıllı
semanticscholar +1 more source
Expanding the Phenotypic Spectrum of Degcags Syndrome: Novel Craniofacial and Oral Findings
ABSTRACT Aims: Developmental delay with gastrointestinal, cardiovascular, genitourinary, and skeletal abnormalities (DEGCAGS) syndrome (OMIM #619488) is a rare autosomal recessive disorder caused by pathogenic variants in ZNF699 and characterized by developmental delay and multisystem involvement.
Jeferson Paiva +8 more
wiley +1 more source
This work overcomes Poisson's ratio limitations in piezoresistive sensors via strain‐adaptive liquid metal (LM) interfaces. EGaIn‐coated TPU scaffolds enable directional LM flow to fill microcracks under deformation, achieving ultra‐high sensitivity (693.65 kPa-1).
Yuxiao Zhang +10 more
wiley +1 more source
Tetraploid–diploid mosaicism in humans is exceedingly rare. We present an 11‐year‐old boy with tetraploid–diploid mosaicism and coexistent hair hypopigmentation with skin hypo‐ and hyperpigmentation. This case expands the current literature as we are not aware of previous documentation of this unique combination of pigmentary anomalies.
John Paul Schacht +3 more
wiley +1 more source
Objective To investigate the correlation between positional skull deformation (PD) and motor performance of infants under 4 months of age. Methods Infants aged under 4 months were enrolled in the children’s healthcare and the premature infants follow-up ...
Tianqi Huang +10 more
doaj +1 more source

