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

C536942

Orphanet Code

ORPHA:2886
TARP syndrome
MeSHC536942
OrphanetORPHA:2886
Treatments0 drug(s)
Symptoms on record55 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO