Results 121 to 130 of about 265,457 (270)
American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 728-732, March 2026.ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source
Oral myiasis in a cerebral palsy patient: a case report [PDF]
, 2010 Myiasis is a rare condition caused by the invasion of tissues by the larvae of flies, mainly from the order of Diptera. Many cases of myiasis involving various human organs have been reported. Oral Myiasis is very rare in healthy persons.
Gupta, S. +3 more
core +1 more source
BMC Oral Health, 2015 BackgroundAmelogenesis imperfecta represents a group of developmental conditions, clinically and genetically heterogeneous, that affect the structure and clinical appearance of enamel. Amelogenesis imperfecta occurred as an isolated trait or as part of a
I. Cherkaoui Jaouad +5 more
semanticscholar +1 more source
Stem Cell Therapy for Inflammatory Diseases: Progress, Challenges, and Future Directions
MedComm, Volume 7, Issue 2, February 2026.Stem cells offer multifaceted therapeutic approaches for inflammatory diseases, each exhibiting distinct therapeutic properties. Hematopoietic stem cells, primarily through hematopoietic stem cell transplantation (HSCT), can effectively remodel the immune environment, showing particular promise in treating genetically linked cases.
Chen Wu +4 more
wiley +1 more source
Juvenile hyaline fibromatosis: A 10-year follow-up
Indian Journal of Dermatology, 2017 Juvenile hyaline fibromatosis (JHF) is a rare hereditary disease with an autosomal recessive transmission. JHF is characterized by papulonodular skin lesions, osteolytic bone lesions, flexural joint contractures, and gingival hyperplasia and usually ...
Esra Baltacioglu +6 more
doaj +1 more source
Pulp Polyp Associated with a Natal Tooth: Case Report [PDF]
, 2009 Natal teeth are an infrequent occurrence at birth. Often these teeth are extracted because they are very mobile and pose a risk of aspiration. This is a rare case in which a natal tooth was extracted by the pediatrician with his fingers.
Hodgson, Brian D. +2 more
core +1 more source
Cell Proliferation, Volume 59, Issue 2, February 2026.FAM20A variants cause AI1G, marked by enamel defects, gingival overgrowth and ectopic calcifications. RNA sequencing of patient‐derived gingival fibroblasts showed dysregulated genes in adhesion, proliferation and signalling pathways. Functional assays revealed increased cell proliferation, impaired ECM interactions and osteogenesis, suggesting FAM20A ...
Kanokwan Sriwattanapong +9 more
wiley +1 more source
Management of amlodipine-induced gingival enlargement: Series of three cases
Journal of Indian Society of Periodontology, 2010 Gingival enlargement is one of the side effects associated with certain drugs. Amlodipine, a calcium channel blocker, used as antihypertensive drug has been found associated with gingival hyperplasia. This case series presents diagnosis and management of
Srivastava Amit +3 more
doaj
Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
Case Reports in Dentistry, 2011 This is a case report of a patient with idiopathic gingival hyperplasia and an undiagnosed genetic disorder that demonstrated static encephalopathy, mental retardation, developmental delay, seizures, hypotonia, and severe gingival hypertrophy.
Bien Lai +2 more
doaj +1 more source
Non syndromic gingival fibromatosis in a mild mental retardation child
Contemporary Clinical Dentistry, 2012 Gingival fibromatosis is a benign oral condition characterized by enlargement of gingival tissues. It usually develops as an isolated disorder but can be one of the features of a syndrome.
Mahesh K Duddu +3 more
doaj +1 more source