agammaglobulinemia/edema

Lyen an sove nan clipboard la

Atik Esè klinikPatant

Chwazi kalite sòt

Paj 1 soti nan 44 rezilta yo

[Lymphoid leukosis with agammaglobulinemia and anasarca].

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Clinical-pathological conference. Progressive generalized edema in an 8-year-old boy with agammaglobulinemia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

[Idiopathic hypoproteinemia with hypogammaglobulinemia; normo-aldosteronic edema; polyglobulia].

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Hypogammaglobulinemia with facial edema.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

[A case of rheumatoid arthritis complicated with prolonged pneumonia and pulmonary edema possibly caused by gold sodium thiomalate-induced hypogammaglobulinemia].

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Erythroderma with spongiotic dermatitis. Association with common variable hypogammaglobulinemia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Two middle-aged men presented with generalized erythroderma, diffuse alopecia, and hyperkeratosis of the palms and soles. Histopathologic study demonstrated spongiosis (epidermal intercellular edema) with a perivascular lymphohistiocytic infiltrate. Complete immunologic evaluation demonstrated that

Streptococcal sepsis presenting as acute abdomen in a child with transient hypogammaglobulinemia of infancy.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Group A streptococcal sepsis was documented in a child who presented with an acute abdomen. Massive retroperitoneal edema was observed at laparotomy with no focus of infection. Immunologic evaluation revealed low serum immunoglobulins and deficient in vitro IgG synthesis consistent with transient

Tonsillar granuloma associated with hypogammaglobulinemia

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Background: Rare tonsillar granulomas may be caused for example by infections, malignancies or sarcoidosis. Granulomas also occur in inborn errors of immunity (IEI) such as common variable immunodeficiency (CVID) with B cell maturation

Familial enteropathy with villous edema and immunoglobulin G2 subclass deficiency.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

We describe a familial form of recurrent acute, life-threatening secretory diarrhea associated with distinctive jejunal histologic changes and IgG2 subclass deficiency. Symptoms begin abruptly with anorexia and vomiting, and progress within hours to massive secretory diarrhea and shock with profound

Spontaneous repigmentation of silvery hair in an infant with congenital hydrops fetalis and hypoproteinemia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Silvery hair is a characteristic finding of 3 rare autosomal recessive disorders: Chédiak-Higashi syndrome (CHS), Elejalde syndrome (ES), and Griscelli syndrome (GS). We report the case of a 2-month-old male infant with transient silvery hair and generalized hypopigmentation of the skin and eyes who

Renal amyloidosis in a patient with X-linked agammaglobulinemia (Bruton's disease) and bronchiectasis.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

OBJECTIVE We present a patient with Bruton's disease and bronchiectasis who developed renal AA amyloidosis. METHODS A 38 year-old man was diagnosed with X-linked agammaglobulinemia (Bruton's disease) when he was 3 years old, and he has been treated with parenteral immunoglobulin since then. Eighteen

Shulman disease (eosinophilic fasciitis) in X-linked agammaglobulinemia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

X-linked agammaglobulinemia (XLA) diagnosed in the first year of life is an immunodeficiency with a life-long indication for substitution of immunoglobulins, due to lack of B lymphocytes in the periphery. The decrease of bacterial infection frequency and severity is an effect of immunoglobulin

Transient hypogammaglobulinemia in the adult. Functional assessment of T and B lymphocytes.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

The woman described suffered from a pruritic erythematous rash, edema, malaise and fever which appeared during Tegretol therapy. The patient was shown to have a severe hypogammaglobulinemia with absence of circulating B lymphocytes, but normal cell-mediated immunity. There was an absence of in vitro

Recurrent pulmonary alveolar proteinosis secondary to agammaglobulinemia.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

Pulmonary alveolar proteinosis (PAP) is characterized by the accumulation of surfactant derived material in the lung of patients. PAP is rare in children. The patient presented with respiratory failure. In the history she was diagnosed with agammaglobulinemia at 8 months of age and has been treated

Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality.

Se sèlman itilizatè ki anrejistre yo ki ka tradwi atik yo

In this report, we describe a brother and sister who presented at birth with short-limb skeletal dysplasia, polyhydramnios, prematurity, and generalized edema. Dysmorphic features included broad nose, thick ears, thin lips, micrognathia, inverted nipples, ulnar deviation at the wrists, spatulate

Antre nan paj
facebook nou an

Herbal & Natural Medicine

Baz done ki pi konplè remèd fèy medsin te apiye nan syans

Travay nan 55 lang
Geri èrbal te apiye nan syans
Remèd fèy rekonesans pa imaj
Kat entèaktif GPS - tag zèb sou kote (vini byento)
Li piblikasyon syantifik ki gen rapò ak rechèch ou an
Search remèd fèy medsin pa efè yo
Izeganize enterè ou yo ak rete kanpe fè dat ak rechèch la nouvèl, esè klinik ak rive

Tape yon sentòm oswa yon maladi epi li sou remèd fèy ki ta ka ede, tape yon zèb ak wè maladi ak sentòm li itilize kont.
* Tout enfòmasyon baze sou rechèch syantifik pibliye