Glossary for Nasal voice
Medical terms related to Nasal voice or mentioned in this section include:
- Adenoiditis: Infection of the adenoids in the nasal-throat region
- Blepharophimosis telecanthus microstomia: A rare syndrome characterized by a flat face, small mouth and ear anomaly as well as a range of other abnormalities.
- Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of the upper lip.
- Branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and: A rare genetic disorder characterized by branchial defects, tear duct obstruction and pseudocleft of upper lip.
- Branchio-Oculo-Facial Syndrome: A rare genetic disorder characterized by branchial defects, lacrimal duct obstruction and pseudocleft of upper lip.
- Breath symptoms: Breath-related symptoms including breath odor
- Breathing symptoms: Symptoms affecting the breathing systems.
- Chromosome 22q11 Deletion Spectrum: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
- Chromosome 2p16.1-p15 Deletion Syndrome: A rare genetic disorder characterized by a range of manifestations including mental retardation and skull and facial anomalies.
- Chronic Sinusitis: Chronic inflammation of the sinuses
- Chronic sinusitis: Chronic inflammation of the sinuses
- Cold-like symptoms: Symptoms similar to the common cold.
- Common cold: Symptoms similar to the common cold.
- Communication symptoms: Symptoms related to problems with communication.
- Deletion 22q11: A rare chromosomal disorder where a small piece of genetic material is missing from chromosome 22 at the q11 location.
- Deviated Septum: A septum in the nose that is deviated from the normal position
- Dextrocardia-bronchiectasis-sinusitis: A genetic disorder characterized by sinusitis, bronchiectasis and situs inversus.
- DiGeorge syndrome: 22q11.2 deletion syndrome is a genetic disorder which can result in a vast array of symptoms. Various names have been used to describe different manifestations of the syndrome. Di George Syndrome primarily involves an underdeveloped thymus and parathyroid glands which results in lowered immunity low blood calcium levels respectively. Another primary feature is heart defects. Various other variable features are also present. It is not uncommon for patients to have more than one of the 22q11.2 deletion syndrome subtypes which can make diagnosis confusing - other subtypes include Sphrintzen syndrome, Caylor cardiofacial syndrome and CATCH 22.
- Distal myopathy with vocal cord weakness: A very rare syndrome characterized mainly by muscle weakness in the end portion of the arms and legs as well as the vocal cord and pharynx.
- Face symptoms: Symptoms affecting the face
- Flaccid dysarthria: A neurological voice disorder caused by damage or malfunction of the cranial or spinal nerves. May be caused by trauma, surgery, stroke, tumor, infection, degenerative diseases and muscle diseases.
- Freeman-Sheldon Syndrome: A very rare genetic disorder characterized by abnormal development of the skeleton and muscles.
- Head symptoms: Symptoms affecting the head or brain
- Hoarse: Hoarseness or loss of voice
- Hyperkinetic dysarthria: A voice disorder where damage to part of the brain called the basal ganglia affects muscle tone and causes involuntary movements of the muscles involved in speech. May be caused by cancer, infections and Huntington's disease as well as others.
- Hypotonia-cystinuria syndrome: A genetic disorder characterized by reduced muscle tone, growth hormone deficiency and unusual facial appearance. Failure to thrive occurs during the first years of life but is replaced by rapid weight gain in later childhood. This syndrome is a milder form of the 2p21 deletion syndrome.
- Juvenile dermatomyositis: A very rare autoimmune disorder where the body's own immune system attacks blood vessels and causes them to become inflamed. The condition is characterized by progressive muscle weakness and a characteristic pinkish-purple rash.
- Larynx symptoms: Symptoms affecting the larynx (voice box) in the neck
- Limb-girdle muscular dystrophy type 1A: An autosomal dominant form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the myotilin gene.
- Mouth symptoms: Symptoms of the mouth or oral area.
- Myasthenia Gravis: An autoimmune disorder which interferes with nerve impulses to muscles and hence results in weak, easily fatigued muscles.
- Myopathy, Myofibrillar, BAG3-Related: An early-onset, progressive muscle disease.
- Nasal polyp: A polyp that is found in the nasal passage
- Neck symptoms: Symptoms affecting the neck
- Nose conditions: Any condition that affects the nose
- Nose symptoms: Symptoms affecting the nose
- Oral submucous fibrosis: A rare disorder involving inflammation and progressive fibrosis of tissues inside the mouth. The condition starts with redness, blistering and ulceration inside the mouth that is eventually replaced with stiff fibrous tissue as it heals. The inside of the mouth can become stiff and hinder oral functions such as eating, speaking and even opening the mouth. Even the pharynx may occasionally be involved. The condition can become cancerous. The disorder is often associated with chewing betel nuts in Asian and Indian areas.
- Polio: Dangerous virus now rare due to vaccination.
- Pterygium syndrome multiple dominant type: A very rare syndrome characterized by joint contractures, finger webbing, difficulty fully opening mouth and scoliosis.
- Respiratory symptoms: Symptoms affecting the breathing systems.
- Shprintzen syndorme: An inherited syndrome of cardiac defects and craniofacial anomalies and various other abnormalities.
- Simosa craniofacial syndrome: A rare disorder characterized by a range of facial anomalies including a high forehead, long face, flat face and a small mouth.
- Snyder-Robinson syndrome: A rare syndrome characterized by mental retardation, reduced muscle tone, abnormal walk, weak bones and an asymmetrical face.
- Spasmodic dysphonia: A psychogenic voice disorder which has neurological origins. The vocal fold muscles spasm involuntarily during speech. May be caused by psychological factors as well as other conditions.
- Speech symptoms: Problems with speech or voice.
- Spinal bulbar motor neuropathy: A rare inherited disease that affects the nerves in the spine and in the bulbous (bulbar) part of the brain stem. The main signs are muscle weakness and wasting.
- Stuffed nose: Blockage to the nose often from runny nose
- Throat symptoms: Symptoms affecting the throat
- Velocardiofacial syndrome: A genetic disorder which can present with a wide range of phenotypic manifestations which has lead to a number of different names being assigned to the various presentations e.g. DiGeorge Syndrome and Cayler Anomaly Face Syndrome. There are nearly 200 different symptoms that can occur and the severity of the condition is also highly variable depending on the nature and severity of the symptoms that are present.
- Velofacioskeletal syndrome: A ver rare sydnrome characterized mainly by short stature and facial and skeletal abnormalities.
- Verloes-David Syndrome: An inherited condition characterised by shortness of stature and multiple skeletal abnormalities.
- Voice changes: Any changes which occur to ones voice
- Voice symptoms: Symptoms affecting the voice
Conditions listing medical symptoms: Nasal voice:
The following list of conditions
have 'Nasal voice' or similar
listed as a symptom in our database.
This computer-generated list may be inaccurate or incomplete.
Always seek prompt professional medical advice about the cause
of any symptom.
Select from the following alphabetical view of conditions which
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Conditions listing medical complications: Nasal voice:
The following list of medical conditions have 'Nasal voice'
or similar listed as a medical complication in our database.
Nov 21, 2003
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