Results 241 to 250 of about 35,818 (311)

Longitudinal Behavior Phenotype Hallmarks in RNU4‐2 Syndrome: Implications for Clinical Management

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 201, Issue 3, Page 205-211, April 2026.
ABSTRACT Pathogenic variants in the non‐coding spliceosomal gene RNU4‐2 underlie ReNU syndrome, one of the most prevalent monogenic causes of neurodevelopmental disorders, accounting for ~0.4% of cases. Despite increasing recognition, little is known about the longitudinal behavioral and neuropsychiatric phenotype of affected individuals. We report two
Paola Francesca Ajmone   +8 more
wiley   +1 more source

Triplication of deciduous teeth: a rare dental anomaly.

open access: yesNiger J Surg, 2013
Yadav S, Tyagi S, Kumar P, Sharma D.
europepmc   +1 more source

Radicular Cyst in the Lower Right Primary Tooth and Its Management: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Radicular cysts are the most common inflammatory odontogenic cysts but are relatively uncommon in the primary dentition. When present, they may cause significant destruction and adversely affect the eruption of permanent teeth. A 6‐year‐old boy presented with painful swelling in the right mandibular buccal region.
Fahimeh Anbari   +4 more
wiley   +1 more source

Early Oral Rehabilitation of a Pediatric Patient With Hypohidrotic Ectodermal Dysplasia: A Case Report from Afghanistan

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Hypohidrotic ectodermal dysplasia (HED) is a rare congenital disorder characterized by abnormal development of ectodermal structures including hair, teeth, nails, and sweat glands. Dental manifestations such as anodontia or hypodontia can significantly impair mastication, speech development, facial esthetics, and psychosocial well‐being ...
Nazera Ahmadzai   +5 more
wiley   +1 more source

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