GTS5:SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2): Difference between revisions

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==Related Terminology==
==Related Terminology==
<span style="color:#0070C0">(''Instructions: This table will have the related terminology from the WHO book <u>autocompleted</u>.)''</span>
 
{| class="wikitable"
{| class="wikitable"
|+
|+
|Acceptable
|Acceptable
|
|Hereditary paraganglioma-phaeochromocytoma syndromes 1 to 5 (PGL1, PGL2, PGL3, PGL4, PGL5); Carney triad (restricted to syndromic but non-hereditary disease)
|-
|-
|Not Recommended
|Not Recommended
|
|N/A
|}
|}
Not Recommended:  Carney-Stratakis dyad/syndrome


==Definition/Description of Disease==
==Definition/Description of Disease==
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