-
Omenn syndrome is an
autosomal recessive severe combined immunodeficiency. It is ****ociated with
hypomorphic missense mutations in
immunologically relevant...
-
Gilbert S.
Omenn is an
American medical doctor and researcher. He
currently is the
Harold T.
Shapiro Distinguished University Professor at the University...
- PMID 39133222.
Goodman GE,
Thornquist MD,
Balmes J,
Cullen MR,
Meyskens FL,
Omenn GS, et al. (December 2004). "The Beta-Carotene and
Retinol Efficacy Trial:...
-
endocrine autoimmune diseases.
APECED causes loss of
central immune tolerance.
Omenn syndrome manifests as GVHD (graft
versus host disease)-like
autoimmune disease...
- Med. 330 (15): 1029–35. doi:10.1056/NEJM199404143301501. PMID 8127329.
Omenn GS,
Goodman GE,
Thornquist MD, et al. (1996). "Risk
factors for lung cancer...
-
syndrome Nezelof syndrome (thymic
dysplasia with
normal immunoglobulins)
Omenn syndrome Purine nucleoside phosphorylase deficiency Severe combined immunodeficiency...
-
hypotrichosis (MDWH),
anauxetic dysplasia (AD),
kyphomelic dysplasia (KD),
Omenn syndrome (OS) are
diseases ****ociated with
mutated and (or) dysfunctional...
-
insufficiency of T cells, such as
severe combined immunodeficiency (SCID),
Omenn syndrome, and Cartilage–hair hypoplasia.
Secondary causes are more common...
- SPINK5, and TYK2 (see
mutations in the
hymperimmoglobulin E syndrome).
Omenn syndrome is a
severe combined immunodeficiency disease characterized by...
- PMID 8127329.
Goodman GE,
Thornquist MD,
Balmes J,
Cullen MR,
Meyskens FL,
Omenn GS, et al. (December 2004). "The Beta-Carotene and
Retinol Efficacy Trial:...
