Sandbox:Ali: Difference between revisions
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=== Primary immunodeficiency: === | === Primary immunodeficiency: === | ||
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!Primary immunodeficiency disorders | |||
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|Phagocyte cell defects | |||
|Decreased number | |||
Functional Defects | |||
|Schwachman-Diamond Syndrome | |||
G6PC3 deficiency | |||
Cohen Syndrome | |||
Barth Syndrome | |||
Glycogen Storage Disease Type 1b | |||
Clericuzio Syndrome | |||
VPS45 deficiency | |||
P14/LAMTOR2 deficiency | |||
JAGN1 deficiency | |||
3-methylglutaconic aciduria | |||
SMARCD2 deficiency | |||
WDR1 deficiency | |||
HYOU1 deficiency | |||
Elastase deficiency | |||
HAX1 deficiency(Kostmann Disease) | |||
GFI1 deficiency | |||
G-CSF receptor deficiency | |||
X-linked neutropenia /mylodysplasia WAS GOF | |||
Neutropenia with combined immune deficiency | |||
Cystic Fibrosis | |||
Papillion-Lefèvre | |||
Localized juvenile peridontitis | |||
B-Actin | |||
Leukocyte adhesion deficiency | |||
GATA2 def (MonoMac sd) | |||
Specific granule deficiency | |||
Pulmonary alveolar proteinosis | |||
Chronic Granulomatous Disease | |||
Rac 2 def | |||
G6PD def Class 1 | |||
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|Defects in Intrinsic and Innate immunity | |||
|Predisposition to bacterial infections | |||
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{{Reflist|2}} | {{Reflist|2}} |
Revision as of 19:07, 4 October 2018
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ali Akram, M.B.B.S.[2]
Overview
Classification
Immunodeficiency disorders are classified into two types:
- Primary immunodeficiency
- Secondary immunodeficiency
Primary immunodeficiency:
Primary immunodeficiency disorders | ||||
---|---|---|---|---|
Phagocyte cell defects | Decreased number
Functional Defects |
Schwachman-Diamond Syndrome
G6PC3 deficiency Cohen Syndrome Barth Syndrome Glycogen Storage Disease Type 1b Clericuzio Syndrome VPS45 deficiency P14/LAMTOR2 deficiency JAGN1 deficiency 3-methylglutaconic aciduria SMARCD2 deficiency WDR1 deficiency HYOU1 deficiency Elastase deficiency HAX1 deficiency(Kostmann Disease) GFI1 deficiency G-CSF receptor deficiency X-linked neutropenia /mylodysplasia WAS GOF Neutropenia with combined immune deficiency Cystic Fibrosis Papillion-Lefèvre Localized juvenile peridontitis B-Actin Leukocyte adhesion deficiency GATA2 def (MonoMac sd) Specific granule deficiency Pulmonary alveolar proteinosis Chronic Granulomatous Disease Rac 2 def G6PD def Class 1 |
||
Defects in Intrinsic and Innate immunity | Predisposition to bacterial infections | |||