TARP syndrome
MeSH: C536942ORPHA: 2886
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with TARP syndrome, sourced from HPO and Orphanet clinical annotations.
Pierre-Robin sequenceAtrial septal defectTalipes equinovarusPersistent left superior vena cavaGlossoptosisCleft palateHypertelorismSloping foreheadMicrognathiaWide nasal bridgeCyanosisIntellectual disabilityGlobal developmental delayGeneralized hypotoniaFailure to thriveIntrauterine growth retardationRocker bottom footUnderdeveloped supraorbital ridgesCryptorchidismHorseshoe kidneyHydronephrosisLarge fontanellesHearing impairmentSmall earlobeProminent antihelixAnteverted naresMyopiaThick eyebrowSingle transverse palmar creaseHand polydactylySeizureAbnormal corpus callosum morphologyCerebellar hypoplasiaExtramedullary hematopoiesisApneaBroad-based gaitScoliosisWidely patent fontanelles and suturesFinger syndactylyHypoplasia of proximal radiusAbnormal antihelix morphologyShort palpebral fissureClinodactylyTongue nodulesOptic atrophyPectus excavatumShort sternumTetralogy of FallotPulmonary hypoplasiaAbnormal duodenum morphologyAlveolar ridge overgrowthAbnormal hair patternAthetoid cerebral palsyPostaxial polydactylyPosteriorly rotated ears
Classification & Codes
MeSH Code
C536942Orphanet Code
ORPHA:2886TARP syndrome
| MeSH | C536942 |
| Orphanet | ORPHA:2886 |
| Treatments | 0 drug(s) |
| Symptoms on record | 55 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO