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Tunnused
Geeniga SPART seotud tunnused
spartin
Inimese fenotüübi ontoloogia seostab geeniga SPART 74 tunnust kehasüsteemide kaupa: omadusi, mida täheldatakse inimestel, kellel on selle geeni üks haruldastest seisunditest.
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Abnormality of the nervous system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Babinski sign | Alati |
| Difficulty articulating speech | Alati |
| Impaired vibration sensation at ankles | Alati |
| Increased reflexes | Alati |
| Intellectual disability, mild | Alati |
| Lack of coordination of movement | Alati |
| Motor delay | Alati |
| Abnormal shape of brain | Sageli (30–79%) |
| Abnormality of the cerebellum | Sageli (30–79%) |
| Cognitive impairment | Sageli (30–79%) |
| Delayed speech and language development | Sageli (30–79%) |
| Global developmental delay | Sageli (30–79%) |
| Impaired vibratory sensation | Sageli (30–79%) |
| Slurred speech | Sageli (30–79%) |
| Specific learning disability | Sageli (30–79%) |
| Anxiety | Mõnikord (5–29%) |
| Can't control feelings | Mõnikord (5–29%) |
| Difficulty sleeping | Mõnikord (5–29%) |
| Hallucinations | Mõnikord (5–29%) |
| Panic attack | Mõnikord (5–29%) |
| Psychosis | Mõnikord (5–29%) |
| Speech apraxia | Mõnikord (5–29%) |
| Abnormal gait | Pole registreeritud |
| Degeneration of cerebellum | Pole registreeritud |
| Knee clonus | Pole registreeritud |
Abnormality of the musculoskeletal system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Distal muscle wasting | Alati |
| Hyperextensible hand joints | Alati |
| Kyphoscoliosis | Alati |
| Lower limb spasticity | Alati |
| Spastic paraplegia | Alati |
| Spastic walk | Alati |
| Abnormality of the skeletal system | Sageli (30–79%) |
| Double-Jointed | Sageli (30–79%) |
| Generalized decreased muscle tone | Sageli (30–79%) |
| Involuntary muscle stiffness, contraction, or spasm | Sageli (30–79%) |
| Muscle degeneration | Sageli (30–79%) |
| Spastic dysarthria | Sageli (30–79%) |
| Spastic paraparesis | Sageli (30–79%) |
| Flexed joint that cannot be straightened | Pole registreeritud |
| Permanent flexion of the finger or toe | Pole registreeritud |
| Uncontrollable movement in upper arms | Pole registreeritud |
Abnormality of limbs
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| High-arched foot | Alati |
| Lower limb muscle weakness | Alati |
| Short foot | Alati |
| Ulnar deviation of the hand | Alati |
| Abnormal feet structure | Sageli (30–79%) |
| Abnormal shape of hand | Sageli (30–79%) |
| Abnormality of the hand | Sageli (30–79%) |
| Decreased arm strength | Sageli (30–79%) |
| Abnormal rhythmic movements of ankle | Mõnikord (5–29%) |
| Abnormality of the thumb | Mõnikord (5–29%) |
| Curvature of digit | Mõnikord (5–29%) |
| Knock knees | Mõnikord (5–29%) |
| Hammertoe | Pole registreeritud |
| Short fingers or toes | Pole registreeritud |
Abnormality of head or neck
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Deep bite | Sageli (30–79%) |
| Abnormality of the nostrils | Mõnikord (5–29%) |
| Abnormally small head | Mõnikord (5–29%) |
| Downward slanting of the opening between the eyelids | Mõnikord (5–29%) |
| Eye folds | Mõnikord (5–29%) |
| Prominent nose | Mõnikord (5–29%) |
| Big midface | Pole registreeritud |
| Drooling | Pole registreeritud |
Abnormality of the digestive system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Chronic constipation | Alati |
| Poor swallowing | Alati |
| Constipation | Sageli (30–79%) |
Abnormality of the genitourinary system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Dull burning sensation with urination | Sageli (30–79%) |
| Hydronephrosis | Harva (1–4%) |
| Urinary urgency | Pole registreeritud |
Growth abnormality
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Growth delay | Sageli (30–79%) |
| Short stature | Sageli (30–79%) |
Abnormality of the ear
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Low-set ears | Mõnikord (5–29%) |
Abnormality of the eye
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Wide-set eyes | Sageli (30–79%) |
Abnormality of the voice
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Hoarse voice | Mõnikord (5–29%) |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: geeniga SPART seotud tunnused ja iga tunnuse esinemissagedus. Lisateavet leiate aadressilt hpo.jax.org.
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