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

C537923

Orphanet Code

ORPHA:93932
FG syndrome
MeSHC537923
OrphanetORPHA:93932
Treatments0 drug(s)
Symptoms on record72 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO