Results 101 to 110 of about 5,413 (278)

Pattern and Factors Associated with Congenital Anomalies among Young Infants Admitted at Bugando Medical Centre, Mwanza, Tanzania. [PDF]

, 2014
Congenital anomalies or birth defects are among the leading causes of infant mortality and morbidity around the world. The impact of congenital anomalies is particularly severe in middle- and low-income countries where health care resources are limited ...
Chalya, Phillipo L, Kidenya, Benson R, Manyama, Mange, Mashuda, Florentina, Zuechner, Antke   +4 more
core   +1 more source

Lingual Papillae in Hamdani Sheep During Foetal Periods: Gross, Scanning Electron Microscopy, Histochemical and Immunohistochemical Analysis

Veterinary Medicine and Science, Volume 11, Issue 4, July 2025.
*First Trimester: Tongue development began, and lingual papillae appeared as primordium. *Second Trimester: The tongue grew, and primitive taste buds and papilla structures formed. *Third Trimester: Lingual papillae became prominent, and taste buds and serous glands were detected.
Barış Can Güzel, İhsan Işbilir, Senem Esin Yavaş, Fatma Işbilir   +3 more
wiley   +1 more source

Oral health care pathways for patients with epidermolysis bullosa: A position statement from the European reference network for rare skin diseases

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 6, Page 1080-1090, June 2025.
The European Reference Network for Rare Skin Diseases has developed consensus‐based oral health care pathways for dental referral, treatment and follow‐up for patients with EB according to their risk for oral and dental manifestations and complications. Referral for early preventive strategies is key to reducing the burden of disease.
S. Krämer, A. L. Hillebrecht, K. Bekes, K. Bücher, V. Clark, H. Haririan, J. Jakowski, C. Joseph, N. Meißner, J. Monteiro, S. Porter, R. Schilke, S. Veliz, V. Verhaeghe, A. Vinereanu, M. C. Bolling, A. Diem, J. E. Mellerio, C. Bodemer, C. Has   +19 more
wiley   +1 more source

Nonrecurrent Triplication of 5q21.3q23.3: A Case Report and Review of the Literature

American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.
ABSTRACT Triplications involving 5q21.3q23.3 are rare, and a phenotype has not been established. Here, we present a 4‐month‐old male with dysmorphic facial features and congenital cardiac malformation. Chromosomal microarray identified a pathogenic triplication of 5q21.3q23.3 with chromosome analysis showing the extra 5q material inserted into 16q ...
Jacob A. Ginter, Sarah Beaudry, Natalya Guseva, Jaime Nagy, Aaron A. Stence, Alpa Sidhu   +5 more
wiley   +1 more source

Oropalatal dysplasia: A case report with an innovative sequence of reconstruction

Journal of Cleft Lip Palate and Craniofacial Anomalies, 2014
A rare syndromic cleft palate child with microstomia and ankyloglossia is presented. The child presented at 1-month of age with microstomia, complete cleft of the secondary palate, ankyloglossia with dorsal groove of the tongue.
Karoon Agrawal, Sanjay Kumar, Rakesh Kumar Srivastava, Mukund Gupta   +3 more
doaj   +1 more source

A novel de novo TBX5 mutation in a patient with Holt-Oram syndrome leading to a dramatically reduced biological function [PDF]

, 2016
BACKGROUND: The Holt-Oram syndrome (HOS) is an autosomal dominant disorder affecting 1/100.000 live births. It is defined by upper limb anomalies and congenital heart defects with variable severity.
Cleuziou, Julie, Deutsch, Marcus-André, Doppler, Stefanie, Dreßen, Martina, Ewert, Peter, Krane, Markus, Lahm, Armin, Lahm, Harald, Lange, Rüdiger, Malčić, Ivan, Pabst von Ohain, Jelena, Schön, Patric, Wolf, Klaudia   +12 more
core   +1 more source

Assessing ankyloglossia: Prevalence, complications, and the controversy of frenotomy

International Journal of Applied Dental Sciences
Introduction: Ankyloglossia, or a short lingual frenulum, can interfere with breastfeeding, harming the infant's development, injuring the mother's nipples, and prompting early discontinuation of nursing.
Mariana Villfranca Cantu, R. S. Nájera, Jaime Adrián Mendoza Tijerina, Hilda Hortencia Hermelinda Torre Martínez, Maria del Carmen Theriot Giron, María Concepción Treviño Tijerina, Aurora Lucero Reyes, Elvia Ortiz Ortiz, Juan Manuel Solís Soto   +8 more
semanticscholar   +1 more source

Transformative Dental Care in Pediatric Moebius Syndrome: Bridging Oral Health and Systemic Management During Prolonged Hospitalization

Special Care in Dentistry, Volume 45, Issue 3, May/June 2025.
ABSTRACT Moebius syndrome is a rare congenital disorder of unknown etiology. It is characterized by non‐progressive paralysis of the facial and abducens cranial nerves due to atrophy of their nuclei, often accompanied by malformations in the upper and lower limbs.
Renata Zoraida Rizental Delgado, Marcus Bueno, Leda Mugayar, Juliana Bertoldi Franco   +3 more
wiley   +1 more source

A closer look at ankyloglossia in children—A case series

Journal of Dr. NTR University of Health Sciences
Ankyloglossia, often known as tongue-tie, is characterized by a small lingual frenum that obstructs normal tongue movement. It is a rare congenital oral abnormality. The most significant clinical symptom of movement restriction is evaluated clinically by
Krishna P. Vellore, Saigeeta Kondamadugu, Santosh K. Challa, Mayuri Ganesh, Kanchan Kumari, Deepanshi Sharma, Treyi Bartarya   +6 more
doaj   +1 more source

Caso clínico: tumor glómico agresivo de localización lingual [PDF]

, 2004
El tumor glómico es una neoplasia benigna que se origina en las células musculares lisas del glomus vascular. Los glomagiomas de cabeza y cuello son raros, con una incidencia del 0,6%.
González Lagunas, Javier, Quesada, Roger, Raspall Martín, Guillermo   +2 more
core   +1 more source