Delineating the phenotype of 1p36 deletion in adolescents and adults. Issue 10 (8th July 2014)
- Record Type:
- Journal Article
- Title:
- Delineating the phenotype of 1p36 deletion in adolescents and adults. Issue 10 (8th July 2014)
- Main Title:
- Delineating the phenotype of 1p36 deletion in adolescents and adults
- Authors:
- Brazil, Ashley
Stanford, Kevin
Smolarek, Teresa
Hopkin, Robert - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga36657-sec-0001" sec-type="section"> <p>1p36 deletion is the most common telomeric deletion syndrome, with an incidence of 1/5, 000–1/10, 000. A variety of clinical complications have been reported including seizures, hypotonia, heart malformations, cardiomyopathy, vision problems, and hearing loss. Approximately 90% are reported to have severe to profound intellectual disability and 75% to have absent expressive language. Little is known about long‐term outcomes. The current literature suggests a poor prognosis for most patients. This study attempted to assess medical conditions and function of adolescent and adult patients with 1p36 deletion. A survey was distributed through three support groups to identify patients &gt;12 years of age to assess functional status and medical problems in older patients with 1p36 deletion syndrome. 40 patients were identified between 12 and 46 years old. Among our survey sample, medical complications including seizures, hypotonia, structural heart defects, hearing loss, and vision problems, were similar to previous reports. However, functional skills were better than anticipated, with an overwhelming majority reported to independently sit, walk, and receive the majority of nutrition orally. Forty‐four percent were reported to use complex speech abilities. While medical problems in patients with 1p36 deletion were similar to those that have been<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga36657-sec-0001" sec-type="section"> <p>1p36 deletion is the most common telomeric deletion syndrome, with an incidence of 1/5, 000–1/10, 000. A variety of clinical complications have been reported including seizures, hypotonia, heart malformations, cardiomyopathy, vision problems, and hearing loss. Approximately 90% are reported to have severe to profound intellectual disability and 75% to have absent expressive language. Little is known about long‐term outcomes. The current literature suggests a poor prognosis for most patients. This study attempted to assess medical conditions and function of adolescent and adult patients with 1p36 deletion. A survey was distributed through three support groups to identify patients &gt;12 years of age to assess functional status and medical problems in older patients with 1p36 deletion syndrome. 40 patients were identified between 12 and 46 years old. Among our survey sample, medical complications including seizures, hypotonia, structural heart defects, hearing loss, and vision problems, were similar to previous reports. However, functional skills were better than anticipated, with an overwhelming majority reported to independently sit, walk, and receive the majority of nutrition orally. Forty‐four percent were reported to use complex speech abilities. While medical problems in patients with 1p36 deletion were similar to those that have been previously reported, we also demonstrated these same concerns persist into adolescence and adulthood. Additionally, patients were reported to have better functional skills than anticipated. Thus, quality of life and level of function appear to be better than anticipated from previous studies. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of medical genetics. Volume 164:Issue 10(2014.)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 164:Issue 10(2014.)
- Issue Display:
- Volume 164, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 164
- Issue:
- 10
- Issue Sort Value:
- 2014-0164-0010-0000
- Page Start:
- 2496
- Page End:
- 2503
- Publication Date:
- 2014-07-08
- Subjects:
- Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.36657 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3539.xml