Characterization of facial phenotypes of children with congenital hypopituitarism and their parents: A matched case‐control study. (5th April 2015)
- Record Type:
- Journal Article
- Title:
- Characterization of facial phenotypes of children with congenital hypopituitarism and their parents: A matched case‐control study. (5th April 2015)
- Main Title:
- Characterization of facial phenotypes of children with congenital hypopituitarism and their parents: A matched case‐control study
- Authors:
- Manousaki, Despoina
Allanson, Judith
Wolf, Lior
Deal, Cheri - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga37069-sec-0001" sec-type="section"> <p>Congenital Hypopituitarism (CH) has traditionally been associated with specific facial phenotypes subsumed under the term midface retrusion, based on cephalometric studies. In this study, we used a systematic anthropometric approach to facial morphology in 37 individuals with CH and their parents, primarily of French Canadian ancestry, and compared them to a control group of 78 French Canadian patients with well‐controlled type 1 diabetes and their parents. We were able to demonstrate clear morphological differences, which were more prevalent in the affected group than in the control group. More specifically, we showed the presence of a shorter skull base width (<italic>P</italic> &lt; 0.001) and reduced inner canthal distance (<italic>P</italic> = 0.006) in the CH face, as well as a relative underdevelopment of the mandible (<italic>P</italic> = 0.001). These findings were present in individuals of all ages, and were independent of the duration of growth hormone treatment (median treatment 90.8 months; range 7.2–175.8 months). In addition, skull base width was significantly reduced in both mothers and fathers of affected children compared to the parents of the controls (<italic>P </italic>&lt; 0.001), despite comparable parental heights, supporting an underlying genetic etiology. Such extensive phenotypic studies have not<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga37069-sec-0001" sec-type="section"> <p>Congenital Hypopituitarism (CH) has traditionally been associated with specific facial phenotypes subsumed under the term midface retrusion, based on cephalometric studies. In this study, we used a systematic anthropometric approach to facial morphology in 37 individuals with CH and their parents, primarily of French Canadian ancestry, and compared them to a control group of 78 French Canadian patients with well‐controlled type 1 diabetes and their parents. We were able to demonstrate clear morphological differences, which were more prevalent in the affected group than in the control group. More specifically, we showed the presence of a shorter skull base width (<italic>P</italic> &lt; 0.001) and reduced inner canthal distance (<italic>P</italic> = 0.006) in the CH face, as well as a relative underdevelopment of the mandible (<italic>P</italic> = 0.001). These findings were present in individuals of all ages, and were independent of the duration of growth hormone treatment (median treatment 90.8 months; range 7.2–175.8 months). In addition, skull base width was significantly reduced in both mothers and fathers of affected children compared to the parents of the controls (<italic>P </italic>&lt; 0.001), despite comparable parental heights, supporting an underlying genetic etiology. Such extensive phenotypic studies have not been done in congenital hypopituitarism and will provide further opportunities for data mining. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- American journal of medical genetics. Volume 167:Number 7(2015:Jul.)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 167:Number 7(2015:Jul.)
- Issue Display:
- Volume 167, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 167
- Issue:
- 7
- Issue Sort Value:
- 2015-0167-0007-0000
- Page Start:
- 1525
- Page End:
- 1533
- Publication Date:
- 2015-04-05
- Subjects:
- Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.37069 ↗
- 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:
- 3135.xml