growth delay due to insulin-like growth factor type 1 deficiency
MeSH: C563867ORPHA: 73272
Overview
Growth delay due to insulin-like growth factor I deficiency is characterised by the association of intrauterine and postnatal growth retardation with sensorineural deafness and intellectual deficit
Available Treatments (0)
No treatments linked yet
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Clinical Presentation
Signs and symptoms associated with growth delay due to insulin-like growth factor type 1 deficiency, sourced from HPO and Orphanet clinical annotations.
MicrocephalyPrelingual sensorineural hearing impairmentSensorineural hearing impairmentAtypical behaviorShort attention spanHyperactivityInsulin resistanceIntellectual disabilityMild intellectual disabilityFailure to thriveIntrauterine growth retardationSmall for gestational ageAbnormal facial shapeShort statureAttention deficit hyperactivity disorderCongenital sensorineural hearing impairmentBilateral sensorineural hearing impairmentSevere intrauterine growth retardationSevere postnatal growth retardationPostnatal growth retardationHypogonadismAbnormality of the mouthMicrognathiaDelayed eruption of teethOsteoporosisDelayed skeletal maturationNeonatal hyperbilirubinemiaClinodactyly of the 5th fingerSmall placentaClinodactylyLow anterior hairlinePtosisMyopiaSingle transverse palmar creaseCafe-au-lait spotMotor delayHypoglycemiaTruncal obesityLow posterior hairlineCongenital bilateral ptosisConcave nasal ridgeProminent forehead
Classification & Codes
MeSH Code
C563867Orphanet Code
ORPHA:73272growth delay due to insulin-like growth factor type 1 deficiency
| MeSH | C563867 |
| Orphanet | ORPHA:73272 |
| Treatments | 0 drug(s) |
| Symptoms on record | 42 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO