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{{Family tree | | | | | B01 | | | | | | | | | | B02 | | | | | | | | | | | | | | | | | | | | |B01=CD19 NL: SCID T-ve B+ve|B02=CD19 ↓: SCID T-ve B-ve}}
{{Family tree | | | | | B01 | | | | | | | | | | B02 | | | | | | | | | | | | | | | | | | | | |B01=CD19 NL: SCID T-ve B+ve|B02=CD19 ↓: SCID T-ve B-ve}}
{{Family tree | | |,|-|-|^|-|-|.| | | | | |,|-|-|^|-|-|.| | | | | | | | | | | | | | | | |}}
{{Family tree | | |,|-|-|^|-|-|.| | | | | |,|-|-|^|-|-|.| | | | | | | | | | | | | | | | |}}
{{Family tree | | C01 | | | | C02 | | | | C03 | | | | C04 | | | | | | | | | | | | | | | | |}}
{{Family tree | | C01 | | | | C02 | | | | C03 | | | | C04 | | | | | | | | | | | | | | | | |C01=SCID T-B+NK-|C02=SCID T-B+NK+|C03=SCID T-B-NK-|C04=SCID T-B-NK=}}
{{Family tree | |!| | | | | |!| | | | | |!| | | | | |,|^|-|-|-|.| | | | | | |}}
{{Family tree | |!| | | | | |!| | | | | |!| | | | | |,|^|-|-|-|.| | | | | | |}}
{{Family tree | |)| D01 | | |)| E01 | | |)| F01 | | G01 | | | G02 | | | | | | | |}}
{{Family tree | |)| D01 | | |)| E01 | | |)| F01 | | G01 | | | G02 | | | | | | | |}}

Revision as of 12:58, 5 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

\

Algorithms

 
 
 
 
 
 
 
 
 
 
Immunodeficiency affecting cellular and humoral immunity
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
CD19 NL: SCID T-ve B+ve
 
 
 
 
 
 
 
 
 
CD19 ↓: SCID T-ve B-ve
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
SCID T-B+NK-
 
 
 
SCID T-B+NK+
 
 
 
SCID T-B-NK-
 
 
 
SCID T-B-NK=
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
{{{ D01 }}}
 
 
 
 
{{{ E01 }}}
 
 
 
 
{{{ F01 }}}
 
{{{ G01 }}}
 
 
{{{ G02 }}}
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
{{{ D02 }}}
 
 
 
 
{{{ E02 }}}
 
 
 
 
{{{ F02 }}}
 
 
 
{{{ H01 }}}
 
 
 
{{{ H05 }}}
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
{{{ E03 }}}
 
 
 
 
 
 
 
 
 
{{{ H02 }}}
 
 
 
{{{ H06 }}}
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
{{{ E04 }}}
 
 
 
 
 
 
 
 
 
{{{ H03 }}}
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
{{{ E05 }}}
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

=References