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Microspherophakia with hernia

MedGen UID:
322521
•Concept ID:
C1834881
•
Disease or Syndrome
Synonym: MICROSPHEROPHAKIA WITH HERNIA
 
Monarch Initiative: MONDO:0007997
OMIM®: 157150

Recent clinical studies

Prognosis

A homozygous mutation in LTBP2 causes isolated microspherophakia.
Kumar A, Duvvari MR, Prabhakaran VC, Shetty JS, Murthy GJ, Blanton SH
Hum Genet 2010 Oct;128(4):365-71. Epub 2010 Jul 9 doi: 10.1007/s00439-010-0858-8. PMID: 20617341

Clinical prediction guides

A homozygous mutation in LTBP2 causes isolated microspherophakia.
Kumar A, Duvvari MR, Prabhakaran VC, Shetty JS, Murthy GJ, Blanton SH
Hum Genet 2010 Oct;128(4):365-71. Epub 2010 Jul 9 doi: 10.1007/s00439-010-0858-8. PMID: 20617341

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