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Pseudoleprechaunism syndrome, Patterson type

MedGen UID:
358350
Concept ID:
C1868546
Disease or Syndrome
Synonym: Patterson's leprechaunoid syndrome
SNOMED CT: Patterson syndrome (771262009); Pseudoleprechaunism syndrome Patterson type (771262009); Patterson pseudoleprechaunism syndrome (771262009)
 
Monarch Initiative: MONDO:0008211
OMIM®: 169170
Orphanet: ORPHA2976

Definition

A rare genetic adrenal disorder with characteristics of congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism and severe intellectual disability. Patients additionally present hyperadrenocorticism, cushingoid features, premature adrenarche and diabetes mellitus, as well as skeletal deformities (not present at birth and which progress with age). There have been no further descriptions in the literature since 1981. [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVPseudoleprechaunism syndrome, Patterson type
Follow this link to review classifications for Pseudoleprechaunism syndrome, Patterson type in Orphanet.

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