IP is an uncommon X-linked dominant disorder (incidence: 1/40.000 newborn). It is caused by mutations in NEMO. It is characterized by cutaneous lesions and dental, ocular, neurologic, nails, hair disorders. The ocular and neurologic sequelae represent the major morbidity in IP. We present a case-report with classical cutaneous features diagnostic for IP. The clinical, ophtalomologic and neurologic examinations revealed no other pathological manifestations
Incontinentia pigmenti : case report / D. Portaleone, E. Taroni, S. Micheli, M. Moioli, A. Pedrazzini, V. Carnelli. - In: PEDIATRIA MEDICA E CHIRURGICA. - ISSN 0391-5387. - 29:6(2007), pp. 343-345.
Incontinentia pigmenti : case report
V. CarnelliUltimo
2007
Abstract
IP is an uncommon X-linked dominant disorder (incidence: 1/40.000 newborn). It is caused by mutations in NEMO. It is characterized by cutaneous lesions and dental, ocular, neurologic, nails, hair disorders. The ocular and neurologic sequelae represent the major morbidity in IP. We present a case-report with classical cutaneous features diagnostic for IP. The clinical, ophtalomologic and neurologic examinations revealed no other pathological manifestations
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