FG syndrome
MeSH: C537923ORPHA: 93932
Overview
disease
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 FG syndrome, sourced from HPO and Orphanet clinical annotations.
Inguinal herniaCryptorchidismHypospadiasWide mouthHigh palateMacrocephalyProminent occiputMalar flatteningHypertelorismLong philtrumMicrognathiaHigh foreheadCupped earStenosis of the external auditory canalProminent noseBroad neckStrabismusDownslanted palpebral fissuresOptic nerve hypoplasiaDental crowdingDelayed speech and language developmentAbnormal sternum morphologyGlobal developmental delayAbnormal cerebellum morphologyPlagiocephalySlender buildPremature birthAtrial septal defectPes planusBroad toePyloric stenosisVentriculomegalyBroad-based gaitFrontal upsweep of hairAbnormal large intestine morphologyDroolingModerate intellectual disabilityGeneralized joint hypermobilityShort statureWidely patent fontanelles and suturesMalrotation of colonLimited elbow extension and supinationAplasia/Hypoplasia of the corpus callosumMicrotiaGeneralized neonatal hypotoniaFused teethThick vermilion borderSmall pituitary glandOpen mouthHydrocephalusShort chinSensorineural hearing impairmentChoanal atresiaCompulsive behaviorsSingle transverse palmar creaseSacral dimpleAbnormal thumb morphologySeizureCraniosynostosisUmbilical herniaMitral valve prolapseCoarctation of aortaConstipationGastroesophageal refluxAnal atresiaPulmonary arterial hypertensionProgressive flexion contracturesFinger syndactylyAttention deficit hyperactivity disorderFacial wrinklingAbnormal social behaviorClinodactyly of the 2nd finger
Classification & Codes
MeSH Code
C537923Orphanet Code
ORPHA:93932FG syndrome
| MeSH | C537923 |
| Orphanet | ORPHA:93932 |
| Treatments | 0 drug(s) |
| Symptoms on record | 72 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO