Its "non-syndromic" designation means the hearing loss has not previously been linked to any other medical conditions.

Non-syndromic autism categorizes autistic patients for which there is no known cause.

They successfully cloned the first non-syndromic deafness-related gene in 1999.

Mutations in this gene have been shown to cause non-syndromic mental retardation.

Non-syndromic are more common and affected patients usually present with a large head, seizures and developmental delay.

Snowflake was diagnosed by scientists as having non-syndromic albinism.

(The term "non-syndromic obesity" is sometimes used to exclude these conditions.)

Non-syndromic RP usually presents a variety of the following symptoms:

These anomalies are associated with X-linked non-syndromic deafness.

Non-isolated cases included both syndromic and non-syndromic clefts.

Most examples of radioulnar synostosis are isolated (non-syndromic).

Mutations in the SLC26A5 gene have been associated with non-syndromic hearing loss.

TBX22 mutations also result in non-syndromic cleft palate in some populations.

It is the first time that a specific genetic mutation has been linked to a non-syndromic form of urinary tract malformation.

Increased risk for non-syndromic cleft palate among infants exposed to lamotrigine during pregnancy (abstract).

Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder.

In cases where clefting is the only symptom, a complete family history must be taken to ensure the patient does not have non-syndromic clefting.

Pectus carinatum is generally a solitary, non-syndromic abnormality.

Non-syndromic oral clefts are considered 'complex' or 'multifactorial' in that both genes and environmental factors contribute to the etiology.

Genetic mutations causing a large portion of non-syndromic deafness have been described, offering the potential for improving both diagnosis and therapy.

Craniosynostosis where no extracranial deformations are present, is called non-syndromic or 'isolated' craniosynostosis.

Although WBS is a rare disorder, many of the symptoms are seen in other patient groups in non-syndromic forms.

Studies have noted the association between both developmental delay and non-syndromic autism and enlarged or dilated perivascular spaces.

Snowflake was a Western Lowland Gorilla with non-syndromic oculocutaneous albinism.

Two substitution mutations, Arg196Pro and Met61Lys cause only familial non-syndromic tooth agenesis.