Young syndrome

Common Name(s)

Young syndrome

Young syndrome is a condition whose signs and symptoms may be similar to those seen in cystic fibrosis, including bronchiectasis, sinusitis, and obstructive azoospermia (a condition in which sperm are produced but do not mix with the rest of the ejaculatory fluid due to a physical obstruction, resulting in nonexistent levels of sperm in semen) . The condition is usually diagnosed in middle-aged men who undergo evaluation for infertility. Although the exact cause has not been identified, it is believed to be a genetic condition. At this time, there is no known effective treatment or cure for Young syndrome.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Young syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Young syndrome" returned 399 free, full-text research articles on human participants. First 3 results:

Marshall syndrome in a young child, a reality: Case report.
 

Author(s): Laura Mihaela Trandafir, Madalina Ionela Chiriac, Smaranda Diaconescu, Ileana Ioniuc, Ingrith Miron, Daniel Rusu

Journal: Medicine (Baltimore). 2016 Nov;95(44):e5065.

 

Recurrent fever syndrome, known as the Marshall syndrome (MS), is a clinical entity that includes several clinical features, such as: fever (39-40°C) that occurs repeatedly at variable intervals (3-8 weeks) and in episodes of 3 to 6 days, cervical adenopathy, pharyngitis, and aphthous ...

Last Updated: 18 Nov 2016

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Juvenile polyposis syndrome: An unusual case report of anemia and gastrointestinal bleeding in young infant.
 

Author(s): Yi-Han Hsiao, Chin-Hung Wei, Szu-Wen Chang, Lung Chang, Yu-Wei Fu, Hung-Chang Lee, Hsuan-Liang Liu, Chun-Yan Yeung

Journal: Medicine (Baltimore). 2016 Sep;95(37):e4550.

 

Juvenile polyposis syndrome, a rare disorder in children, is characterized with multiple hamartomatous polyps in alimentary tract. A variety of manifestations include bleeding, intussusception, or polyp prolapse. In this study, we present an 8-month-old male infant of juvenile polyposis ...

Last Updated: 16 Sep 2016

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Triglycerides to High-Density Lipoprotein Cholesterol Ratio Can Predict Impaired Glucose Tolerance in Young Women with Polycystic Ovary Syndrome.
 

Author(s): Do Kyeong Song, Hyejin Lee, Yeon Ah Sung, Jee Young Oh

Journal: Yonsei Med. J.. 2016 Nov;57(6):1404-11.

 

The triglycerides to high-density lipoprotein cholesterol (TG/HDL-C) ratio could be related to insulin resistance (IR). We previously reported that Korean women with polycystic ovary syndrome (PCOS) had a high prevalence of impaired glucose tolerance (IGT). We aimed to determine the ...

Last Updated: 5 Sep 2016

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Young syndrome" returned 17 free, full-text review articles on human participants. First 3 results:

Chronic intermittent abdominal pain in young woman with intestinal malrotation, Fitz-Hugh-Curtis Syndrome and appendiceal neuroendocrine tumor: a rare case report and literature review.
 

Author(s): Alessia Cusimano, Ahmed Mohammed Alaaeldien Beniamin Abdelghany, Andrea Donadini

Journal:

 

There are a lot of different causes of abdominal pain; in this case, a young woman suffers from three diseases with similar symptoms. Adult intestinal mal-rotation is a rare condition of deviation from the normal 270° counter clockwise rotation of the midgut resulting in, not only ...

Last Updated: 18 Jan 2016

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A Systematic Review on the Cost-Effectiveness of Genetic and Electrocardiogram Testing for Long QT Syndrome in Infants and Young Adults.
 

Author(s): Fernando Matias Gonzalez, Maria Assunta Veneziano, Anna Puggina, Stefania Boccia

Journal: Value Health. 2015 Jul;18(5):700-8.

 

Recent improvements in the identification of the genetic basis of long QT syndrome (LQTS) have led to significant changes in the diagnosis and management of this life-threatening condition. Genetic and electrocardiogram (ECG) tests are the most relevant examples among testing strategies ...

Last Updated: 22 Aug 2015

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Cervical neuroendocrine tumor in a young female with Lynch Syndrome.
 

Author(s): Ibraheem Yousef, Fadi Siyam, Lester Layfield, Carl Freter, James R Sowers

Journal: Neuro Endocrinol. Lett.. 2014 ;35(2):89-94.

 

Neuroendocrine tumors rarely occur in the cervix or other components of the reproductive system. These tumors have been associated with microsatellite instability, are very aggressive and often associated with poor outcome. Lynch syndrome is an inherited cancer syndrome that has also ...

Last Updated: 7 Jul 2014

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Risk of Diabetes in Young Turner Syndrome Patients
 

Status: Recruiting

Condition Summary: Turner Syndrome

 

Last Updated: 25 Sep 2015

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Multicenter Evaluation of Children and Young Adults With Genotype Positive Long QT Syndrome
 

Status: Recruiting

Condition Summary: Long QT Syndrome

 

Last Updated: 16 Dec 2016

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