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Craniofaciofrontodigital syndrome

MedGen UID:
393947
Concept ID:
C2676032
Disease or Syndrome
Synonym: CANTU CRANIOFACIOFRONTODIGITAL SYNDROME
SNOMED CT: Craniofaciofrontodigital syndrome (763320005); Cantu craniofaciofrontodigital syndrome (763320005)
Modes of inheritance:
Unknown inheritance
MedGen UID:
989040
Concept ID:
CN307042
Finding
Source: Orphanet
Hereditary clinical entity whose mode of inheritance is unknown.
 
Monarch Initiative: MONDO:0007259
OMIM®: 114620
Orphanet: ORPHA363705

Definition

A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlaxity, wrinkled palms and soles and skeletal anomalies (sella turcica, wide ribs and small vertebral bodies). [from SNOMEDCT_US]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVCraniofaciofrontodigital syndrome
Follow this link to review classifications for Craniofaciofrontodigital syndrome in Orphanet.

Recent clinical studies

Therapy

Myers A, Godden C
BMJ Case Rep 2010 Jul 15;2010 doi: 10.1136/bcr.09.2009.2264. PMID: 22752833Free PMC Article

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