Literature DB >> 28553001

Hypohidrotic Ectodermal Dysplasia: Breastfeeding Complications Due to Impaired Breast Development.

Mandy Wahlbuhl-Becker1, Florian Faschingbauer2, Matthias W Beckmann2, Holm Schneider1.   

Abstract

Background X-linked hypohidrotic ectodermal dysplasia (XLHED), the most common form of ectodermal dysplasia, is caused by mutations in the gene EDA. While only affected men develop the full-blown clinical picture, females who are heterozygous for an EDA mutation often also show symptoms such as hypodontia, hypotrichosis and hypohidrosis. These women may also suffer from malformations of the mammary gland which represent not just a cosmetic problem but can limit their breastfeeding capability. This paper summarizes the findings of the first systematic study on the impact of hypohidrotic ectodermal dysplasia on breastfeeding. Patients Thirty-eight adult female members of the German-Swiss-Austrian ectodermal dysplasia patient support group participated in a structured interview; most of them also agreed to a photodocumentation of their mammary region. Thirty-one women carried mutations in EDA (Group A) and seven were affected by other forms of hypohidrotic ectodermal dysplasia (Group B). Results 39 % of the women of Group A reported that their breasts were of different size or entirely absent on one side. In Group B, 86 % of the women reported differently sized or even absent breasts; two of these women lacked both breasts entirely. Most women described their nipples as exceptionally flat. 10 % of the women of Group A had more than two nipples. The high percentage of deviations from the norm was confirmed in the photodocumentation. Both groups had few or no sebaceous glands of Montgomery in the areolar region. Around 80 % of interviewed women had children and had attempted to breastfeed their first child. 67 % of the mothers in Group A had had difficulty in breastfeeding their infants and generally attributed this difficulty to their flat nipples. All of the mothers in Group B reported difficulties in breastfeeding; 60 % had not been able to breastfeed their first child. Conclusion Mothers with hypohidrotic ectodermal dysplasia very often have difficulty in breastfeeding because of their impaired breast development. This causal relationship needs to be taken into account in lactation counseling.

Entities:  

Keywords:  areola; breast; breastfeeding routine; glands of Montgomery; hypohidrotic ectodermal dysplasia; mammary gland

Year:  2017        PMID: 28553001      PMCID: PMC5406230          DOI: 10.1055/s-0043-100106

Source DB:  PubMed          Journal:  Geburtshilfe Frauenheilkd        ISSN: 0016-5751            Impact factor:   2.915


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4.  Human breast areolae as scent organs: morphological data and possible involvement in maternal-neonatal coadaptation.

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Review 6.  TNF superfamily in skin appendage development.

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8.  Conserved features and evolutionary shifts of the EDA signaling pathway involved in vertebrate skin appendage development.

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Journal:  Mol Biol Evol       Date:  2008-02-27       Impact factor: 16.240

9.  Correction of Inverted Nipple Using Subcutaneous Turn-Over Flaps to Create a Tent Suspension-Like Effect.

Authors:  Hii-Sun Jeong; Hye-Kyung Lee
Journal:  PLoS One       Date:  2015-07-24       Impact factor: 3.240

10.  The secretion of areolar (Montgomery's) glands from lactating women elicits selective, unconditional responses in neonates.

Authors:  Sébastien Doucet; Robert Soussignan; Paul Sagot; Benoist Schaal
Journal:  PLoS One       Date:  2009-10-23       Impact factor: 3.240

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1.  Attenuation of Mammary Gland Dysplasia and Feeding Difficulties in Tabby Mice by Fetal Therapy.

Authors:  Mandy Wahlbuhl; Sonia Schuepbach-Mallepell; Christine Kowalczyk-Quintas; Angela Dick; Fabian B Fahlbusch; Pascal Schneider; Holm Schneider
Journal:  J Mammary Gland Biol Neoplasia       Date:  2018-06-01       Impact factor: 2.673

2.  [Detection of EDA gene mutation and phenotypic analysis in patients with hypohidrotic ectodermal dysplasia].

Authors:  J Y Wu; M Yu; S C Sun; Z Z Fan; J L Zheng; L T Zhang; H L Feng; Y Liu; D Han
Journal:  Beijing Da Xue Xue Bao Yi Xue Ban       Date:  2020-12-09

3.  Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome.

Authors:  Dustin Baldridge; Rebecca C Spillmann; Daniel J Wegner; Jennifer A Wambach; Frances V White; Kathleen Sisco; Tomi L Toler; Patricia I Dickson; F Sessions Cole; Vandana Shashi; Dorothy K Grange
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4.  Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.

Authors:  Sigrun Wohlfart; Ralph Meiller; Johanna Hammersen; Jung Park; Johannes Menzel-Severing; Volker O Melichar; Kenneth Huttner; Ramsey Johnson; Florence Porte; Holm Schneider
Journal:  Orphanet J Rare Dis       Date:  2020-01-10       Impact factor: 4.123

5.  Pathogenic EDA Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype-Phenotype: A Correlation Analysis.

Authors:  Yang Han; Xiuli Wang; Liyun Zheng; Tingting Zhu; Yuwei Li; Jiaqi Hong; Congcong Xu; Peiguang Wang; Min Gao
Journal:  Front Genet       Date:  2020-02-04       Impact factor: 4.599

6.  No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.

Authors:  Laura Körber; Holm Schneider; Nicole Fleischer; Sigrun Maier-Wohlfart
Journal:  Orphanet J Rare Dis       Date:  2021-02-23       Impact factor: 4.123

  6 in total

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