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Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 1(AIH1)

MedGen UID:
336846
•Concept ID:
C1845052
•
Disease or Syndrome
Synonym: Amelogenesis imperfecta, X-linked 1
 
OMIM®: 301200

Recent clinical studies

Etiology

A novel mutation in the AMELX gene and multiple crown resorptions.
Lee KE, Lee SK, Jung SE, Song SJ, Cho SH, Lee ZH, Kim JW
Eur J Oral Sci 2011 Dec;119 Suppl 1:324-8. doi: 10.1111/j.1600-0722.2011.00858.x. PMID: 22243263

Prognosis

A novel mutation in the AMELX gene and multiple crown resorptions.
Lee KE, Lee SK, Jung SE, Song SJ, Cho SH, Lee ZH, Kim JW
Eur J Oral Sci 2011 Dec;119 Suppl 1:324-8. doi: 10.1111/j.1600-0722.2011.00858.x. PMID: 22243263

Clinical prediction guides

A novel mutation in the AMELX gene and multiple crown resorptions.
Lee KE, Lee SK, Jung SE, Song SJ, Cho SH, Lee ZH, Kim JW
Eur J Oral Sci 2011 Dec;119 Suppl 1:324-8. doi: 10.1111/j.1600-0722.2011.00858.x. PMID: 22243263

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