Sandbox:Sahar: Difference between revisions

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{{familytree/start |summary=Sample 1}}
 
{{familytree | | | | | | | | A01 |A01=Germ cell}}  
{{CMG}}; {{AE}} {{Sahar}}
{{familytree | | | | |,|-|-|-|^|-|-|-|-|.| | | }}
 
{{familytree | | | B01 | | | | | | | | B02 | | |B01=Pathogenesis|B02=Malignant transformation}}
==Overview==
{{familytree | | | |!| | | | | | | | | |!| }}
 
{{familytree | | | C01 | | | | | | | | |!| |C01=Mature teratoma}}
==Historical Perspective==
{{familytree | | | | | | | | | | | | | |!}}
 
{{familytree | | | | | | | | | |,|-|-|-|+|-|-|-|.| }}
This disease named after the name of ''Martin XXXX''.
{{familytree | | | | | | | | | E01 | | E02 | | E03 |E01=Tumors esxpressing transcription factors of pluripotency|E02=Tumors with primitive embryonic ectoderm, mesoderm, and/or endoderm differentiation|E03=Tumors with extraembroyonic differentiation}}
 
{{familytree | | | | | | | | | |!| | | |!| | | |!| | }}
==Pathophysiology==
{{familytree | | | | | | | | | F01 | | F02 | | F03 | |F01=Dysgerminoma/Embryonal carcinoma|F02=Immature teratoma|F03=Yolk sac tumor/Choriocarcinoma}}
This disease is fif;nkf;n,;nd/;FN<gmnfnl;mfng/lm,h/,fn.<ref name="pmid29322855">{{cite journal| author=Özdel S, Özçakar ZB, Cakar N, Aydın F, Çelikel E, Elhan AH et al.| title=Fatigue in pediatric patients with familial Mediterranean fever. | journal=Mod Rheumatol | year= 2018 | volume= 28 | issue= 6 | pages= 1016-1020 | pmid=29322855 | doi=10.1080/14397595.2018.1427459 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29322855  }} </ref>
{{familytree/end}}
 
==Classification==
Hyperparathyroidism is classified into three categories:
*Primary
*Secondary
**<font color="blue">Psudosecondary</font>
*Tertiary
 
==Dignostic Methods==
 
There are different methods to diagnose this disease.<br>
#Ultrasound<br>
#CT Scan
 
==Radiopedia==
 
[[Image:Acute-pancreatitis-and-walled-off-necrosis.jpg|thumb|center|1024px|Acute pancreatitis - Case courtesy of A.Prof Frank Gaillard, Radiopaedia.org, rID: 29888]]
 
==Treatment==
 
Currently, there is no curative medication for this disease and supportive care is only available.<br>I need my text to be <font color="blue">blue</font>.<br>
Supportive care is described in the following table:
 
{| class="wikitable" style="text-align:left"
|+Alphabetic table
|-
! * !! A !! B !! C
|-
! W
| D || E || F
|-
! X
| G || H || I
|-
! Y
| J || K || L
|-
! Z
| M || N || O
|-
! M
| P || Q || R
|}
 
==References==
{{Reflist|2}}

Revision as of 21:15, 7 March 2019


 
 
 
 
 
 
 
Germ cell
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Pathogenesis
 
 
 
 
 
 
 
Malignant transformation
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Mature teratoma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Tumors esxpressing transcription factors of pluripotency
 
Tumors with primitive embryonic ectoderm, mesoderm, and/or endoderm differentiation
 
Tumors with extraembroyonic differentiation
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Dysgerminoma/Embryonal carcinoma
 
Immature teratoma
 
Yolk sac tumor/Choriocarcinoma
 
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