Cutis verticis gyrata
A rare, autosomal dominant inherited disorder caused by mutations in the FGFR2 gene. It is characterized by the premature fusion of the bones of the skull (craniosynostosis) and a skin abnormality called cutis gyrata. The craniosynostosis results in a cloverleaf-shaped skull, wide-set eyes, ear abnormalities, underdeveloped upper jaw, and developmental delays. Cutis gyrata is characterized by a wrinkled skin appearance, especially on the face, near the ears, and on the palms and soles.
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Ayush Pharmashist
Kanpur Para Medical Institute
d.pharma
20 Years of Teaching To Both UGs & PGs
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Gandhi Medical College, Dr. NTRUHS
MD Pathology
Ruby Hospital Pune EMS Done
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