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Ring 18 chromosome associated with cleft palate: case report and comprehensive literature review of clinical symptoms.
Orphanet J Rare Dis
December 2024
Department of Burns and Plastic Surgery, University Hospital Brno, Jihlavska 20, Brno, 62500, Czech Republic.
Background: Ring 18 chromosome is a rare chromosomal aberration associated with a wide range of symptoms affecting all organ systems. One possible symptom associated with this condition is an orofacial cleft. However, to date, there are very few reported cases where the cleft has been surgically treated.
View Article and Find Full Text PDFEvaluating quality of life changes in patients with cleft lip or palate: a mixed method pre- and postsurgical analysis in Karachi.
BMC Oral Health
December 2024
Fazaia Ruth Pfau Medical College, Karachi, Pakistan.
Background: Cleft lip and/or palate (CLP) is the most common orofacial congenital disability, presenting significant medical, psychological, and social challenges. In Pakistan, the incidence of CLP is high, estimated at one in 523 live births, but accurate data are lacking due to the absence of a birth registry. Early diagnosis and intervention are crucial for improving outcomes.
View Article and Find Full Text PDFAuthor Correction: Automatic detection and visualization of temporomandibular joint effusion with deep neural network.
Sci Rep
December 2024
Department of Computer Science, Hanyang University, Seoul, 04763, Korea.
Correction: Ulman-Macón et al. Morphological Changes of the Suboccipital Musculature in Women with Myofascial Temporomandibular Pain: A Case-Control Study. 2023, 1159.
Life (Basel)
October 2024
Department of Physical Therapy, Universidad San-Pablo CEU, 28660 Madrid, Spain.
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View Article and Find Full Text PDFWalking Ability After Microsurgical Reconstruction of Pediatric Popliteal Pterygium Syndrome-A Case Report.
J Pers Med
November 2024
Department of Hand Surgery, Peripheral Nerve Surgery and Rehabilitation, Clinic of Plastic and Reconstructive Surgery, Burn Center, BG Trauma Center Ludwigshafen, Department of Hand- and Plastic Surgery, University of Heidelberg, 69117 Heidelberg, Germany.
Background: Popliteal pterygium syndrome (PPS) is a rare congenital disorder characterized by orofacial, cutaneous, musculoskeletal, and genital anomalies. Surgical interventions are necessary to address the severe knee flexion contracture and equinovarus deformity, but there are no established treatment guidelines.
Methods: We present the case of a one-year-old patient with PPS and discuss the challenges in managing the knee deformity.
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