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Hallermann-Streiff syndrome

MeSH: D006210ORPHA: 2108

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

congenital disorder

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 Hallermann-Streiff syndrome, sourced from HPO and Orphanet clinical annotations.

Abnormality of the dentitionBrachycephalyConvex nasal ridgeDevelopmental cataractMicrophthalmiaShort ribsRib exostosesAlopeciaFrontal bossingSparse body hairProportionate short statureDermal atrophyReduced bone mineral densitySparse hairAbnormality of the tongueNarrow mouthGlossoptosisAbnormal cranial suture/fontanelle morphologyMalar flatteningMicrognathiaUnderdeveloped nasal alaeVisual impairmentTelecanthusSparse eyelashesNatal toothHigh, narrow palateRecurrent fracturesAbnormality of hair textureSupernumerary toothSparse eyebrowCryptorchidismMicrocephalyChoanal atresiaStrabismusGlaucomaMyopiaUveitisNystagmusHypothyroidismAbnormal skull morphologyIntellectual disabilityCerebellar hypoplasiaCongestive heart failureShort footRespiratory insufficiencyTracheomalaciaAbdominal situs inversusClinodactyly of the 5th fingerAbnormal cardiovascular system morphologySmall hand

Classification & Codes

MeSH Code

D006210

Orphanet Code

ORPHA:2108
Hallermann-Streiff syndrome
MeSHD006210
OrphanetORPHA:2108
Treatments0 drug(s)
Symptoms on record50 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO