Table 4.

Other Allelic Disorders

GenePhenotype
FBN1 FBN1-related Marfan syndrome
Marfan lipodystrophy syndrome (OMIM 616914)
Isolated ectopia lentis (OMIM 129600)
MASS syndrome (OMIM 604308)
Nonsyndromic heritable thoracic aortic disease (See Heritable Thoracic Aortic Disease Overview.)
Stiff skin syndrome (OMIM 184900)
LTBP3 Dental anomalies and short stature (OMIM 601216)

From: Geleophysic Dysplasia

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