Phakomatoses
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Phakomatoses are a group of neurocutaneous disorders characterized by the involvement of structures that arise from the embryonic ectoderm (thus central nervous system, skin, and eyes). Other organs may also be involved.
Pathology
As a group, they are characterized by widespread abnormalities often with characteristic appearances. There are around 30 phakomatoses of which the most important ones are listed here:
-<p><strong>Phakomatoses</strong> are a group of neurocutaneous disorders characterized by the involvement of structures that arise from the embryonic ectoderm (thus central nervous system, skin, and eyes). Other organs may also be involved.</p><p>As a group, they are characterized by widespread abnormalities often with characteristic appearances. There are around 30 phakomatoses of which the most important ones are listed here:</p><ul>- +<p><strong>Phakomatoses</strong> are a group of neurocutaneous disorders characterized by the involvement of structures that arise from the embryonic ectoderm (thus central nervous system, skin, and eyes). Other organs may also be involved.</p><h4>Pathology</h4><p>As a group, they are characterized by widespread abnormalities often with characteristic appearances. There are around 30 phakomatoses of which the most important ones are listed here:</p><ul>
-<a href="/articles/neurofibromatosis-type-1">Neurofibromatosis type I</a> (NF I) </li>- +<a href="/articles/neurofibromatosis-type-1">neurofibromatosis type I</a> (NF I) </li>
-<a href="/articles/neurofibromatosis-type-2-3">Neurofibromatosis type II</a> (NF II) </li>-<li><a href="/articles/tuberous-sclerosis">Tuberous sclerosis </a></li>-<li><a href="/articles/sturge-weber-syndrome-1">Sturge-Weber Syndrome </a></li>- +<a href="/articles/neurofibromatosis-type-2-3">neurofibromatosis type II</a> (NF II) </li>
- +<li><a href="/articles/tuberous-sclerosis">tuberous sclerosis </a></li>
- +<li><a href="/articles/sturge-weber-syndrome-1">Sturge-Weber syndrome </a></li>
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- refs
Sections changed:
- Syndromes
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