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Torchia D, Happle R.
J Am Acad Dermatol. 2023 Oct;89(4):764-773. doi: 10.1016/j.jaad.2020.12.082. Epub 2021 Feb 12.
Phacomatosis spilorosea versus phacomatosis melanorosea: a critical reappraisal of the worldwide literature with updated classification of phacomatosis pigmentovascularis.
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Acta Dermatovenerol Alp Pannonica Adriat. 2021 Mar;30(1):27-30.
The risk of glaucoma associated with phacomatosis cesioflammea and phacomatosis cesioflammeo-marmorata.
Huang S, Yang Y, Ouyang Z, Guo X, Zhan Z, Liu X, Chen Z, Xu J, Yu M.
Eur J Dermatol. 2022 Sep 1;32(5):589-596. doi: 10.1684/ejd.2022.4317.
Phacomatosis pigmentovascularis revisited and reclassified.
Happle R.
Arch Dermatol. 2005 Mar;141(3):385-8. doi: 10.1001/archderm.141.3.385.
Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.
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Am J Med Genet A. 2019 Jun;179(6):966-977. doi: 10.1002/ajmg.a.61134. Epub 2019 Mar 28.
Phacomatosis pigmentovascularis.
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Phacomatosis spilosebacea and cutaneous skeletal hypophosphatemia syndrome.
Torchia D.
Bone. 2023 Mar;168:116649. doi: 10.1016/j.bone.2022.116649. Epub 2022 Dec 20.
Phacomatosis Melanorosea: A Further Case of an Unusual Skin Disorder.
Tekin B, Yucelten D, Happle R.
Acta Derm Venereol. 2016 Feb;96(2):280-2. doi: 10.2340/00015555-2192.
Phacomatosis is Not a Twin-Spot Phenomenon.
van der Merwe EB, Bhika RE, Meyer D.
J Glaucoma. 2020 Feb;29(2):e11. doi: 10.1097/IJG.0000000000001419.
[Phacomatosis or retinal astrocytic hamartomas].
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J Fr Ophtalmol. 2020 Dec;43(10):1096-1097. doi: 10.1016/j.jfo.2020.01.023. Epub 2020 Sep 16.
