occur in the same patient. In some cases they could have patho-physiological changes common to both diseases. Our patient was seen as a result of having an irritating cough with wheezing, mainly at night, for more than a month. Asthma was diagnosed, and he responded favourably to the treatment given. Upon being informed that he had been examined for infertility for 5 years, alpha-1 antitrypsin (AAT) levels were requested. These confirmed that he had a phenotype SZ AAT deficiency. These findings, together with some evidence published recently, suggested that there is a need to rule out AAT deficiency in males with asthma and infertility
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a hereditary disorder involving lungs, characte...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
AbstractObjectiveTo explore the relations that exist between α1-antitrypsin deficiency (AATD) and as...
A young Caucasian female with severe bronchial asthma and Alpha1-antitrypsin (AAT) deficiency, MZ ph...
SummaryThis study was designed to determine the prevalence of asthma and atopy, in a large group of ...
ABSTRACT Male infertility may be linked to respiratory tract disease in conditions such as cystic fi...
Background: Although the etiology and disease mechanisms of asthma and alpha-1 antitrypsin deficienc...
Asthma is driven by an inflammatory response that may impact testicular function. In this cross-sect...
The study of nasal ciliary beat frequency (CBF) and ultrastructure may contribute to the understandi...
SummaryBackgroundPersistent airflow limitation is common among patients with severe asthma, but its ...
Alpha-1 antitrypsin deficiency (AATD) is a hereditary, monogenic disorder with no unique clinical fe...
AbstractSevere α1-anti-trypsin (AAT) deficiency implies a high risk of pulmonary emphysema developme...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Abstract Background and objective Severe alpha1 antitrypsin deficiency has been clearly associated w...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a hereditary disorder involving lungs, characte...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...
AbstractObjectiveTo explore the relations that exist between α1-antitrypsin deficiency (AATD) and as...
A young Caucasian female with severe bronchial asthma and Alpha1-antitrypsin (AAT) deficiency, MZ ph...
SummaryThis study was designed to determine the prevalence of asthma and atopy, in a large group of ...
ABSTRACT Male infertility may be linked to respiratory tract disease in conditions such as cystic fi...
Background: Although the etiology and disease mechanisms of asthma and alpha-1 antitrypsin deficienc...
Asthma is driven by an inflammatory response that may impact testicular function. In this cross-sect...
The study of nasal ciliary beat frequency (CBF) and ultrastructure may contribute to the understandi...
SummaryBackgroundPersistent airflow limitation is common among patients with severe asthma, but its ...
Alpha-1 antitrypsin deficiency (AATD) is a hereditary, monogenic disorder with no unique clinical fe...
AbstractSevere α1-anti-trypsin (AAT) deficiency implies a high risk of pulmonary emphysema developme...
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine a...
Abstract Background and objective Severe alpha1 antitrypsin deficiency has been clearly associated w...
A1AT deficiency- a genetically inherited autosomal codominant disease with more than 120 identified ...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a hereditary disorder involving lungs, characte...
Alpha-1 antitrypsin deficiency is generally suspected in young patients with pulmonary emphysema or ...