-
21
Three-dimensional analysis of facial morphology in nine-year-old children with different unilateral orofacial clefts compared to normative data
Published 2025-01-01“…Average faces were created for five groups (unilateral cleft lip, alveolus, and/or palate (UCL/A/P), fusion and differentiation defects). …”
Get full text
Article -
22
Evaluation of common COL2A1 gene variants in Iranian patients suspected with Stickler syndrome type I
Published 2025-01-01“…As the data displays, the highest phenotype presentation prevalence rate was related to cleft lip and palate, while hemiparesis was the lowest clinical finding among the patients. …”
Get full text
Article -
23
Practice of Oral and Maxillofacial Surgery in Nepal: Its Scope and Influencing Factor
Published 2019-01-01“…Each of oncology, orthognathic surgery, implantology, and cleft lip/palate surgery was performed by <8% of the participants. …”
Get full text
Article -
24
A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype
Published 2023-01-01“…Our patient was a full-term low birth weight (2150 gm) female newborn, showing cleft upper lip and palate (hard and soft palate), bilateral congenital Talipes Equinovarus with rocker bottom foot, microcephaly, atrial septal defect. …”
Get full text
Article -
25
Is There a Noninvasive Source of MSCs Isolated with GMP Methods with Better Osteogenic Potential?
Published 2019-01-01“…A new trend in the treatment for alveolar clefts in patients with cleft lip and palate involves the use of bone tissue engineering strategies to reduce or eliminate the morbidity associated with autologous bone grafting. …”
Get full text
Article -
26
Oral health-related conditions in Ecuador: A temporal trend analysis of hospital discharges from 2000-2023.
Published 2025-01-01“…Malignant tumors of the head, face, and neck were the most common diagnosis attributed to hospital discharges (16.5%), followed by cleft palate (14.5%) and cleft lip (7.8%) and other diseases of the jaws (5.4%). …”
Get full text
Article -
27
-
28
SMARCA4-related Coffin-Siris syndrome in newborn: a case report and literature review
Published 2025-01-01“…ObjectiveOur objective was to examine the clinical and genetic features of Coffin-Siris syndrome resulting from a pathogenic variant in the SMARCA4 gene.MethodsThe clinical data and molecular genetic test results of a newbron with Coffin-Siris syndrome involving a pathogenic variant in the SMARCA4 gene were retrospectively analyzed, and the related literatures were reviewed.ResultsA newborn exhibited inspiratory dyspnea following birth and developmental anomalies (coarse appearance, thick hair, long eyelashes, broad nasal tip, flat nasal bridge, thin upper lip, thick lower lip, digital anomalies, cleft palate, supraglottic laryngeal chondromalacia, stenosis of the left upper bronchus and hypotonia). …”
Get full text
Article -
29
Atypical Craniosynostosis with Torticollis and Neurological Symptoms: A Rhombencephalosynapsis Sequence
Published 2009-01-01Get full text
Article -
30
Awareness and attitudes of pregnant women concerning genetic disorders and pregnancy termination in northeastern Iran
Published 2025-01-01“…Education level was associated with abortion agreement for various conditions, including cleft lip or palate, Alzheimer’s disease, Turner syndrome, cystic fibrosis, phenylketonuria, Huntington’s disease, autism, fragile X syndrome, and epilepsy. …”
Get full text
Article -
31
Prenatal Diagnosis of Bilateral Ectrodactyly and Radial Agenesis Associated with Trisomy 10 Mosaicism
Published 2013-01-01“…A severe clinical syndrome can be defined, comprising ear abnormalities, cleft lip/palate, malformations of eyes, heart, and kidneys, and deformity of hands and feet and most often associated with death neonatally or in early infancy.…”
Get full text
Article -
32
Anthracyclines disaggregate and restore mutant p63 function: a potential therapeutic approach for AEC syndrome
Published 2025-01-01“…Abstract Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome is a rare genetic disorder caused by mutations in the TP63 gene, which encodes a transcription factor essential for epidermal gene expression. …”
Get full text
Article -
33