Pai Syndrome: Median Cleft Lip, Corpus Callosum Lipoma, and Fibroepithelial Skin Tag
نویسندگان
چکیده
Figure 1. Presentation with median cleft lip, widened nasal tip, and fibroepithelial skin polyps.
منابع مشابه
A further patient with Pai syndrome with autosomal dominant inheritance?
We report a patient with median cleft of the upper lip, cutaneous facial polyps, and lipoma of the corpus callosum who represents a further case of Pai syndrome. The father of the patient showed coloboma of the right iris and shared some facial dysmorphism with his son, thus raising the question of autosomal dominant inheritance.
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BACKGROUND Lipoma in nasal region in a case of Pai syndrome is very rare. Very few cases of Pai syndrome with columellar lipoma with extension to septum and tip have been reported till date. CASE PRESENTATION We report a very rare form of nasal lipoma in a case of Pai syndrome with extension to septum and tip in a 4 year old female child. CONCLUSIONS Pai syndrome with columellar lipoma with...
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NNIN REU Site: Nanotechnology Research Center, Georgia Institute of Technology, Atlanta, GA NNIN REU Principal Investigator: Dr. Ravi V. Bellamkonda, Neurological Biomaterials and Cancer Therapeutics Lab, Department of Biomedical Engineering, Georgia Institute of Technology NNIN REU Mentor: Dr. S.Balakrishna Pai, Neurological Biomaterials and Cancer Therapeutics Lab, Department of Biomedical En...
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We describe a de novo apparently balanced reciprocal translocation, 46,X,t(X;16)(q28;q11.2), in a 13 year old girl with median cleft of the upper lip, pedunculated skin masses on the nasal septum, short stature, and mental retardation. Pai syndrome is characterised by median cleft of the upper lip, pedunculated skin mass(es) on the face, and midline lipoma(s) of the central nervous system. The ...
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