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Jones syndrome
Also Known As:
Fibromatosis gingival progressive deafness; Fibromatosis, Gingival, With Progressive Deafness; Gingival fibromatosis with progressive deafness; Gingival fibromatosis with sensorineural hearing loss
Networked:
2
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Otorhinolaryngologic Diseases: 203
Ear Diseases: 261
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Jones syndrome: 2
Nervous System Diseases: 14178
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Jones syndrome: 2
Signs and Symptoms Pathological Conditions
Signs and Symptoms
Neurologic Manifestations: 7102
Sensation Disorders: 117
Hearing Disorders: 325
Hearing Loss: 12265
Deafness: 5416
Jones syndrome: 2
Stomatognathic Diseases: 705
Mouth Diseases: 98
Periodontal Diseases: 9335
Gingival Diseases: 194
Gingival Overgrowth: 806
Gingival Fibromatosis: 45
Jones syndrome: 2
Mouth Abnormalities: 1
Gingival Fibromatosis: 45
Jones syndrome: 2
Stomatognathic System Abnormalities
Mouth Abnormalities: 1
Gingival Fibromatosis: 45
Jones syndrome: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Congenital Abnormalities: 25723
Stomatognathic System Abnormalities
Mouth Abnormalities: 1
Gingival Fibromatosis: 45
Jones syndrome: 2
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Jones syndrome:
1.
Lipids
IBA
06/01/1970 - "
The lipid profiles of the brain in four cases of Nevin-Jones syndrome are described.
"
2.
Elements
IBA
01/01/2023 - "
Exome sequencing identified a repressor element 1-silencing transcription factor (REST, OMIM *600571) (NM_005612.5) c.2670_2673del p.(Glu891Profs*6) heterozygous variant segregating with Jones syndrome in the family.
"
3.
RE1-silencing transcription factor
IBA
01/01/2023 - "
Exome sequencing identified a repressor element 1-silencing transcription factor (REST, OMIM *600571) (NM_005612.5) c.2670_2673del p.(Glu891Profs*6) heterozygous variant segregating with Jones syndrome in the family.
"