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Quoted phrase not found in phrase index: "IFAP syndrome 1, with or without BRESHECK syndrome"
Page 1
Linear lesions reflecting lyonization in women heterozygous for IFAP syndrome (ichthyosis follicularis with atrichia and photophobia).
König A, Happle R. König A, et al. Am J Med Genet. 1999 Aug 6;85(4):365-8. doi: 10.1002/(sici)1096-8628(19990806)85:4<365::aid-ajmg12>3.0.co;2-#. Am J Med Genet. 1999. PMID: 10398262
A diagnosis of IFAP (ichthyosis follicularis with atrichia and photophobia) syndrome was established in a 1-year-old boy with congenital hairlessness, generalized ichthyotic skin changes with follicular hyperkeratoses, and photophobia. ...This is the first re …
A diagnosis of IFAP (ichthyosis follicularis with atrichia and photophobia) syndrome was established in a 1-year-old bo …
Ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome treated with acitretin.
Khandpur S, Bhat R, Ramam M. Khandpur S, et al. J Eur Acad Dermatol Venereol. 2005 Nov;19(6):759-62. doi: 10.1111/j.1468-3083.2005.01318.x. J Eur Acad Dermatol Venereol. 2005. PMID: 16268889
We describe a 3-year-old male patient with the ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome, who developed cutaneous and ocular involvement in infancy. In addition, he had growth retardation and borderline intelligence; no other systemic involve …
We describe a 3-year-old male patient with the ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome, who develope …
Ichthyosis follicularis, alopecia and photophobia syndrome (IFAP): report of the first case with ocular and cutaneous manifestations in Brazil with a favorable response to treatment.
Höpker LM, Ribeiro CG, Oliveira LM, Moreira AT. Höpker LM, et al. Arq Bras Oftalmol. 2011 Jan-Feb;74(1):55-7. doi: 10.1590/s0004-27492011000100013. Arq Bras Oftalmol. 2011. PMID: 21670910 Free article.
Ichthyosis follicular, alopecia, and photophobia (IFAP) syndrome is a rare disease, with possible X-linked mode of inheritance. ...
Ichthyosis follicular, alopecia, and photophobia (IFAP) syndrome is a rare disease, with possible X-linked mode of inheritance …
Ocular findings in ichthyosis follicularis, atrichia, and photophobia syndrome.
Cursiefen C, Schlötzer-Schrehardt U, Holbach LM, Pfeiffer RA, Naumann GO. Cursiefen C, et al. Arch Ophthalmol. 1999 May;117(5):681-4. doi: 10.1001/archopht.117.5.681. Arch Ophthalmol. 1999. PMID: 10326971
Ichthyosis follicularis, atrichia, and photophobia (IFAP) are typical features of a rare neuroichthyosis termed IFAP syndrome. We demonstrate the ultrastructural findings of the eyes from a 33-year-old patient with IFAP syndrome. Clinically, eye …
Ichthyosis follicularis, atrichia, and photophobia (IFAP) are typical features of a rare neuroichthyosis termed IFAP syndro …