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Agammaglobulinemia 5, autosomal dominant(AGM5)

MedGen UID:
462103
Concept ID:
C3150753
Disease or Syndrome
Synonyms: AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT; AGM5
 
Gene (location): LRRC8A (9q34.11)
 
Monarch Initiative: MONDO:0013290
OMIM®: 613506

Definition

Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the LRRC8A gene. [from MONDO]

Clinical features

From HPO
Low-set ears
MedGen UID:
65980
Concept ID:
C0239234
Congenital Abnormality
Upper insertion of the ear to the scalp below an imaginary horizontal line drawn between the inner canthi of the eye and extending posteriorly to the ear.
Agammaglobulinemia
MedGen UID:
168
Concept ID:
C0001768
Disease or Syndrome
A lasting absence of total IgG and total IgA and total IgM in the blood circulation, whereby at most trace quantities can be measured.
High palate
MedGen UID:
66814
Concept ID:
C0240635
Congenital Abnormality
Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective).
Epicanthus
MedGen UID:
151862
Concept ID:
C0678230
Congenital Abnormality
Epicanthus is a condition in which a fold of skin stretches from the upper to the lower eyelid, partially covering the inner canthus. Usher (1935) noted that epicanthus is a normal finding in the fetus of all races. Epicanthus also occurs in association with hereditary ptosis (110100).
Hypertelorism
MedGen UID:
9373
Concept ID:
C0020534
Finding
Although hypertelorism means an excessive distance between any paired organs (e.g., the nipples), the use of the word has come to be confined to ocular hypertelorism. Hypertelorism occurs as an isolated feature and is also a feature of many syndromes, e.g., Opitz G syndrome (see 300000), Greig cephalopolysyndactyly (175700), and Noonan syndrome (163950) (summary by Cohen et al., 1995).

Recent clinical studies

Etiology

Dury S, Colosio C, Etienne I, Anglicheau D, Merieau E, Caillard S, Rivalan J, Thervet E, Essig M, Babinet F, Subra JF, Toubas O, Rieu P, Launois C, Perotin-Collard JM, Lebargy F, Deslée G; Spiesser group
BMC Pulm Med 2015 Nov 7;15:141. doi: 10.1186/s12890-015-0133-9. PMID: 26545860Free PMC Article

Diagnosis

Sasson SC, Corbett A, McLachlan AJ, Chen R, Adelstein SA, Riminton S, Limaye S
J Med Case Rep 2019 Nov 20;13(1):338. doi: 10.1186/s13256-019-2285-3. PMID: 31744540Free PMC Article
Dury S, Colosio C, Etienne I, Anglicheau D, Merieau E, Caillard S, Rivalan J, Thervet E, Essig M, Babinet F, Subra JF, Toubas O, Rieu P, Launois C, Perotin-Collard JM, Lebargy F, Deslée G; Spiesser group
BMC Pulm Med 2015 Nov 7;15:141. doi: 10.1186/s12890-015-0133-9. PMID: 26545860Free PMC Article
Glocker E, Ehl S, Grimbacher B
Curr Opin Pediatr 2007 Dec;19(6):685-92. doi: 10.1097/MOP.0b013e3282f1ddd5. PMID: 18025937

Therapy

Sasson SC, Corbett A, McLachlan AJ, Chen R, Adelstein SA, Riminton S, Limaye S
J Med Case Rep 2019 Nov 20;13(1):338. doi: 10.1186/s13256-019-2285-3. PMID: 31744540Free PMC Article
Dury S, Colosio C, Etienne I, Anglicheau D, Merieau E, Caillard S, Rivalan J, Thervet E, Essig M, Babinet F, Subra JF, Toubas O, Rieu P, Launois C, Perotin-Collard JM, Lebargy F, Deslée G; Spiesser group
BMC Pulm Med 2015 Nov 7;15:141. doi: 10.1186/s12890-015-0133-9. PMID: 26545860Free PMC Article

Clinical prediction guides

Cho K, Yamada M, Agematsu K, Kanegane H, Miyake N, Ueki M, Akimoto T, Kobayashi N, Ikemoto S, Tanino M, Fujita A, Hayasaka I, Miyamoto S, Tanaka-Kubota M, Nakata K, Shiina M, Ogata K, Minakami H, Matsumoto N, Ariga T
Am J Hum Genet 2018 Mar 1;102(3):480-486. Epub 2018 Feb 15 doi: 10.1016/j.ajhg.2018.01.019. PMID: 29455859Free PMC Article
Dury S, Colosio C, Etienne I, Anglicheau D, Merieau E, Caillard S, Rivalan J, Thervet E, Essig M, Babinet F, Subra JF, Toubas O, Rieu P, Launois C, Perotin-Collard JM, Lebargy F, Deslée G; Spiesser group
BMC Pulm Med 2015 Nov 7;15:141. doi: 10.1186/s12890-015-0133-9. PMID: 26545860Free PMC Article

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