Nonsyndromic: Causes & Reasons

Possible Causes for Nonsyndromic

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Nonsyndromic Hearing Impairment Nomenclature. [ncbi.nlm.nih.gov]

Nonsyndromic deafness Other names Non-syndromic genetic deafness Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. [en.wikipedia.org]

Non-Syndromic Ocular Stickler Syndrome Type 1

Name Stickler Syndrome, Type I, Nonsyndromic Ocular Synonyms STICKLER SYNDROME, ATYPICAL | RHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT, INCLUDED; DRRD, INCLUDED, [mousephenotype.org]

[…] pigmentosa + Retinohepatoendocrinologic Syndrome Rhegmatogenous Retinal Detachment, Autosomal Dominant Spondyloocular Syndrome, Autosomal Recessive Stickler Syndrome, Type I, Nonsyndromic [rgd.mcw.edu]

CONCLUSIONS: This is the first description of a nonsyndromic, high myopia-related, recessive RRD without any signs of vitreoretinal degeneration. [pesquisa.bvsalud.org]

Congenital Mandibular Hypoplasia

The nonsyndromic group The rare group of patients with nonsyndromic malformations of the mandible had very little investigations done on it. [jofs.in]

Although mandibular hypoplasia is a common craniofacial anomaly, patients manifesting nonsyndromic congenital mandibular hypoplasia are a rare subgroup. [ncbi.nlm.nih.gov]

Even though mandibular hypoplasia happens to be a normal craniofacial anomaly, patients manifesting nonsyndromic congenital mandibular hypoplasia are a definite rare subgroup [mandibulartori.com]

Deafness, Autosomal Dominant 23

Symptoms - Deafness- autosomal dominant nonsyndromic sensorineural 23 Progressive deafness Causes - Deafness- autosomal dominant nonsyndromic sensorineural 23 Not supplied [checkorphan.org]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [ipfs.io]

Nonsyndromic deafness Other names Non-syndromic genetic deafness Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. [en.wikipedia.org]

Autosomal Recessive Deafness 103

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

GJB2 is the first nonsyndromic sensorineural deafness gene to be identified. [ejo.eg.net]

Autosomal Dominant Deafness 33

nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 13q34 DFNA33 autosomal dominant deafness 33 [wikidata.org]

What is nonsyndromic deafness? Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. [ourmed.org]

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

Autosomal Dominant Deafness 56

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

[…] indicates any form of nonsyndromic autosomal recessive hearing loss, and DFNX indicates any form of nonsyndromic X-linked inherited hearing loss. [bredagenetics.com]

Approximately 70% of the genetically caused hearing loss is nonsyndromic. [arupconsult.com]

Autosomal Recessive Deafness 84B

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

To the Editor: Recently, the pathologic process underlying nonsyndromic forms of inherited hearing impairment has been studied at the molecular level. 1 The previously localized [nejm.org]

Autosomal Dominant Deafness 64

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Autosomal Dominant Nonsyndromic Hearing Impairment Family studies of autosomal dominant nonsyndromic hearing loss have shown that as in autosomal recessive nonsyndromic hearing [consilieregenetica.org]

Autosomal Recessive Deafness 84

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Mutations in GJB2 account for up to 50% of patients with nonsyndromic AR SNHL. [entokey.com]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

Autosomal Recessive Deafness 76

Disease Ontology Browser autosomal recessive nonsyndromic deafness 22 ( DOID:0110480 ) Alliance: disease page Synonyms: autosomal recessive deafness 22; DFNB22 Alt IDs: OMIM [informatics.jax.org]

To the Editor: Recently, the pathologic process underlying nonsyndromic forms of inherited hearing impairment has been studied at the molecular level. 1 The previously localized [nejm.org]

the tested patients had moderate to profound, bilateral, prelingual, nonsyndromic hearing loss. [ejo.eg.net]

Autosomal Recessive Deafness 88

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

nonsyndromic recessive deafness 9; NRSD9 Alt IDs: OMIM:601071, ICD10CM:H90.3 Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset [informatics.jax.org]

Approximately 70% of the genetically caused hearing loss is nonsyndromic. [arupconsult.com]

Autosomal Recessive Deafness 1B

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

What is GJB2-related DFNB1 Nonsyndromic Hearing Loss and Deafness? [counsyl.com]

Autosomal Recessive Deafness 24

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

[…] indicates any form of nonsyndromic autosomal recessive hearing loss, and DFNX indicates any form of nonsyndromic X-linked inherited hearing loss. [bredagenetics.com]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

Autosomal Recessive Deafness 42

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

What is Nonsyndromic Hearing Loss and Deafness DFNB1? Nonsyndromic Hearing Loss and Deafness DFNB1 is an inherited disorder that only affects hearing. [geneaware.clinical.bcm.edu]

Autosomal Recessive Deafness 46

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

Approximately 70% of the genetically caused hearing loss is nonsyndromic. [arupconsult.com]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

Autosomal Recessive Deafness 44

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

Screening for Nonsyndromic Deafness carriers requires molecular genetic testing for DNA mutations. [mazornet.com]

Autosomal Recessive Deafness 22

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 22 ( DOID:0110480 ) Alliance: disease page Synonyms: autosomal recessive deafness 22; DFNB22 Alt IDs: OMIM [informatics.jax.org]

Autosomal Recessive Deafness 38

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

GJB2 is the first nonsyndromic sensorineural deafness gene to be identified. [ejo.eg.net]

This variant is the most common one associated (when present in two copies) with autosomal recessive nonsyndromic hearing loss, i.e. deafness. [snpedia.com]

Autosomal Dominant Deafness 28

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

GJB2 is the first nonsyndromic sensorineural deafness gene to be identified. [ejo.eg.net]

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. [labcorp.com]

Autosomal Recessive Deafness 23

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

Approximately 70% of the genetically caused hearing loss is nonsyndromic. [arupconsult.com]

Disease Ontology Browser autosomal recessive nonsyndromic deafness 12 ( DOID:0110467 ) Alliance: disease page Synonyms: autosomal recessive deafness 12; DFNB12 Alt IDs: OMIM [informatics.jax.org]

Autosomal Dominant Deafness 11

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [ipfs.io]

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

Nonsyndromic deafness Other names Non-syndromic genetic deafness Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. [en.wikipedia.org]

Autosomal Dominant Deafness 9

What is nonsyndromic deafness? Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. [ourmed.org]

When hearing loss results from environmental factors, it is not inherited. isolated deafness nonsyndromic deafness nonsyndromic hearing impairment nonsyndromic hearing loss [ghr.nlm.nih.gov]

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked nonsyndromic deafness, mitochondrial [en.wikipedia.org]

High Myopia-Sensorineural Deafness Syndrome

Nonsyndromic AD Hearing Loss 33. Recessive Nonsyndromic Hearing Loss 34. Nonsyndromic X-Linked Hearing Loss 35. The End 36. …… Thank you for your kind attention. [slideshare.net]

Nonsyndromic genetic sensorineural hearing loss An estimated 70-80% of hereditary hearing loss is nonsyndromic. [emedicine.medscape.com]

Nonsyndromic hearing impairment More than 70% of hereditary hearing loss is nonsyndromic. 61, 62 Disorders discussed in this section are organized by mode of inheritance. [nature.com]

Bilateral Sensorineural Hearing Loss

Here, we present an unusual clinical presentation of nonsyndromic idiopathic gingival fibromatosis with unknown etiology in a 20-year-old female. [mdcan-uath.org]

Present case report highlights the unusual coexistence of nonsyndromic idiopathic gingival fibromatosis. [ijcdc.com]

a mutation in the son of sevenless-1 ( SOS - 1 ) gene has been suggested as a possible cause of isolated (nonsyndromic) gingival fibromatosis. [jisponline.com]

Cleft Palate

[…] as a case-control study by comparing a nonsyndromic cleft palate only group with an independent, healthy, and unaffected control group who were both examined by specialists [ncbi.nlm.nih.gov]

Original Article Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate Corresponding Author E-mail address: tbeaty@jhsph.edu Johns [doi.org]

Abstract Nonsyndromic cleft palate only (nsCPO) is a facial malformation that has a livebirth prevalence of 1 in 2,500. [ncbi.nlm.nih.gov]

Cleft Lip

The genetic loci for nonsyndromic CLP remain poorly characterized. Two families have recently been reported with a chromosome 17p13.3 microduplication and CLP. [ncbi.nlm.nih.gov]

Recent studies reported two sumoylation target genes, MSX1 and TP63, to have achieved genome-wide level significance in tests of association with nonsyndromic clefts. [ncbi.nlm.nih.gov]

Original Article Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate Corresponding Author E-mail address: tbeaty@jhsph.edu Johns [doi.org]

Craniosynostosis

Understand the craniofacial dysmorphology associated with nonsyndromic craniosynostosis. 2. [ncbi.nlm.nih.gov]

Here, the authors present their last 10 years' experience treatment of nonsyndromic single suture craniosynostosis. [ncbi.nlm.nih.gov]

[…] and nonsyndromic craniosynostoses, and allowing for genotype-based prediction of risk of recurrence in some nonsyndromic families. [ncbi.nlm.nih.gov]

Trigonocephaly

OBJECT: The neurobehavioral morbidity of nonsyndromic trigonocephaly is incompletely understood. [ncbi.nlm.nih.gov]

A rare case of a familial form of nonsyndromic trigonocephaly Cite this: The Pan African Medical Journal. 2015;21:264. doi:10.11604/pamj.2015.21.264.6706 Received: 01/04/2015 [panafrican-med-journal.com]

The series was divided into two groups: nonsyndromal trigonocephaly (n = 184) and trigonocephaly associated with other malformations (n = 53). [ncbi.nlm.nih.gov]

Isolated Trigonocephaly

J Craniofac Surg 2009;20:283-286 Di Rocco F, Arnaud E, Renier D: Evolution in the frequency of nonsyndromic craniosynostosis. [karger.com]

Inclusion criteria were treatment-naive children with isolated nonsyndromic trigonocephaly, being treated with standardized frontoorbital advancement in our department. [ncbi.nlm.nih.gov]