Results 101 to 110 of about 59,130 (275)
Case series: Joubert syndrome and eosinophilic esophagitis
Abstract Joubert syndrome (JS) is a rare genetic disorder characterized by developmental abnormalities, particularly in the brainstem and cerebellar vermis, alongside multisystem manifestations such as kidney and liver anomalies, polydactyly, cleft lip or palate, and tongue defects.
Jonathon Schening +5 more
wiley +1 more source
Feasibility of Imaging the Uvula at the Midtrimester Anomaly Ultrasound
Objectives The fetal palate is not routinely imaged as part of the midtrimester fetal anomaly ultrasound, despite being associated with many syndromes. The “equal sign” depicts the lateral borders of the uvula on 2‐dimensional fetal ultrasound. We assessed the feasibility of adding the equal sign to the midtrimester fetal anomaly ultrasound.
Anna Rose Sims +3 more
wiley +1 more source
Objectives In craniofacial disorders (CD) like cleft lip and/or palate (CL/P), Robin sequence (RS) or Down syndrome (DS), an early orthodontic intervention with different palatal plate devices is often applied. However, there are no data on complications
Christina Weismann +9 more
doaj +1 more source
ObjectiveTo investigate the biomechanical effects of maxillary orthodontic treatment on different alveolar bone grafting positions loaded with occlusal forces in an unilateral cleft lip and palate (UCLP) patient.MethodsFinite element analysis was ...
Zhi Zhang +4 more
doaj +1 more source
Characterizing Secondary Velopharyngeal Surgery in Children With Cleft Palate at an Academic Center
In this retrospective study of children undergoing primary palatoplasty at a single academic institution, 10.8% required secondary surgery for velopharyngeal insufficiency. Multivariate analysis demonstrated that private insurance was associated with decreased odds of secondary surgery, while Asian race was associated with increased odds.
Lauren E. Williamson +5 more
wiley +1 more source
Impact of early synchronous lip and palatal repair on speech [PDF]
<b><i>Aims:</i></b> The purpose of this study was to describe articulation and resonance characteristics of Ugandan English-speaking children with cleft lip and palate (CLP) after synchronous lip and palatal closure (Sommerlad ...
Bettens, Kim +7 more
core +1 more source
Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
We report the first documented case of airway involvement in Conradi–Hünermann–Happle syndrome (CDPX2), an X‐linked dominant form of chondrodysplasia punctata caused by pathogenic variants in EBP. A 2‐month‐old female with genetically confirmed CDPX2 developed severe subglottic stenosis and persistent respiratory distress requiring CPAP; cross ...
Enrique G. Villarreal +3 more
wiley +1 more source
Patterns of Cleft Lip and Cleft Palate in Northern Pakistan
Objectives: To determine the frequency of different types of cleft lip and palate, geographical distribution and its association with consanguinity, family history and other syndromes in the Northern Pakistani population. Study design: Descriptive cross-
Mansoor Khan +6 more
doaj +1 more source
EEG Dynamics in Children Before, During and After General Anesthesia
ABSTRACT Background Age‐specific EEG signatures during anesthesia are described in pediatrics, and perioperative monitoring is increasingly advocated; yet most indices and algorithms derive from adult data and may not generalize to early development. Aims The purpose of this study was to characterize perioperative frontal EEGs in young children younger
Maximilian Markus +3 more
wiley +1 more source
Bilateral microform cleft lip [PDF]
Microform cleft lip (MCL), also called congenital healed cleft lip or cleft lip "frustré", is a rare congenital anomaly. MCL has been described as having the characteristic appearance of a typical cleft lip which has been corrected in utero. We present a
Attard Montalto, Simon +2 more
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