Geburtshilfe Frauenheilkd 2017; 77(04): 377-382
DOI: 10.1055/s-0043-100106
GebFra Science
Original Article/Originalarbeit
Georg Thieme Verlag KG Stuttgart · New York

Hypohidrotic Ectodermal Dysplasia: Breastfeeding Complications Due to Impaired Breast Development

Article in several languages: English | deutsch
Mandy Wahlbuhl-Becker
1   Universitätsklinikum Erlangen, Kinder- und Jugendklinik, Kompetenzzentrum für Ektodermale Dysplasien, Erlangen, Germany
,
Florian Faschingbauer
2   Universitätsklinikum Erlangen, Frauenklinik, Erlangen, Germany
,
Matthias W. Beckmann
2   Universitätsklinikum Erlangen, Frauenklinik, Erlangen, Germany
,
Holm Schneider
1   Universitätsklinikum Erlangen, Kinder- und Jugendklinik, Kompetenzzentrum für Ektodermale Dysplasien, Erlangen, Germany
› Author Affiliations
Further Information

Publication History

received 11 August 2016
revised 15 December 2016

accepted 01 January 2017

Publication Date:
26 April 2017 (online)

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.

 
  • References/Literatur

  • 1 Pinheiro M, Freire-Maia N. Ectodermal dysplasias: a clinical classification and a causal review. Am J Med Genet 1994; 532: 153-162
  • 2 Cluzeau C, Hadj-Rabia S, Jambou M. et al. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. Hum Mutat 2011; 32: 70-72
  • 3 Clarke A, Phillips DI, Brown R. et al. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia. Arch Dis Child 1987; 62: 989-996
  • 4 Heckmann U. Die kongenitale bilaterale Amastie bei Mutter und Tochter; Kasuistische Mitteilung. Geburtsh Frauenheilk 1982; 42: 318-320
  • 5 Al Marzouqi F, Michot C, Dos Santos S. et al. Bilateral amastia in a female with X-linked hypohidrotic ectodermal dysplasia. Br J Dermatol 2014; 171: 671-673
  • 6 Wohlfart S, Söder S, Smahi A. et al. A novel missense mutation in the gene EDARADD associated with an unusual phenotype of hypohidrotic ectodermal dysplasia. Am J Med Genet A 2015; 170A: 249-253
  • 7 Haghighi A, Nikuei P, Haghighi-Kakhki H. et al. Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosis. Br J Dermatol 2013; 168: 1353-1356
  • 8 Mégarbané H, Cluzeau C, Bodemer C. et al. Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene. Am J Med Genet A 2008; 146A: 2657-2662
  • 9 Ip S, Chung M, Raman G. et al. Breastfeeding and maternal and infant health outcomes in developed countries. Evid Rep Technol Assess (Full Rep) 2007; 153: 1-186
  • 10 Koletzko B, Bauer CP, Brönstrup A. et al. Säuglingsernährung und Ernährung der stillenden Mutter. Aktualisierte Handlungsempfehlungen des Netzwerks Gesund ins Leben – Netzwerk Junge Familie, ein Projekt von IN FORM. Monatsschr Kinderheilkd 2013; 161: 237-246
  • 11 Lindfors PH, Voutilainen M, Mikkola ML. Ectodysplasin/NF-κB signaling in embryonic mammary gland development. J Mammary Gland Biol Neoplasia 2013; 18: 165-169
  • 12 Pantalacci S, Chaumot A, Benoît G. et al. Conserved features and evolutionary shifts of the EDA signaling pathway involved in vertebrate skin appendage development. Mol Biol Evol 2008; 25: 912-928
  • 13 Mikkola ML. TNF superfamily in skin appendage development. Cytokine Growth Factor Rev 2008; 19: 219-230
  • 14 Pispa J, Mikkola ML, Mustonen T. et al. Ectodysplasin, Edar and TNFRSF19 are expressed in complementary and overlapping patterns during mouse embryogenesis. Gene Expr Patterns 2003; 3: 675-679
  • 15 Keller JP. Hormon- und Fertilisationsstörungen in der Gynäkologie. 4. Aufl.. Berlin, Heidelberg: Springer; 2013
  • 16 Pötzsch O. Statistisches Bundesamt, Wiesbaden – Geburtentrends und Familiensituation in Deutschland. 2013 Online: https://www.destatis.de/DE/Publikationen/Thematisch/Bevoelkerung/HaushalteMikrozensus/Geburtentrends5122203129004.pdf last access: 12.12.2016
  • 17 Przyrembel H. Bundeszentrale für gesundheitliche Aufklärung – Stillen und Muttermilchernährung. Grundlagen, Erfahrungen und Empfehlungen. 2001 Online: http://www.kinderumweltgesundheit.de/index2/pdf/themen/Allergien/60052_1.pdf last access: 12.12.2016
  • 18 Jagfeld EP. Anatomie und Physiologie der weiblichen Brust. In: Jagfeld EP. Hrsg. Frauenheilkunde natürlich – Das Fachbuch für die Praxis. Norderstedt: Books on Demand GmbH; 2014: 131
  • 19 Jackisch C, Schneider HPG. Gutartige Erkrankungen der weiblichen Brust. In: Dudenhausen JW, Schneider HPG, Bastert G. Hrsg. Frauenheilkunde und Geburtshilfe. Berlin: de Gruyter Lehrbuch; 2003: 395-416
  • 20 Göttlicher S. Über die Häufigkeit und Lokalisation von Polythelien, Polymastien und Mammae aberratae. Geburtsh Frauenheilk 1986; 46: 697-699
  • 21 Schaal B, Doucet S, Sagot P. et al. Human breast areolae as scent organs: morphological data and possible involvement in maternal-neonatal coadaptation. Dev Pyschobiol 2006; 2: 100-110
  • 22 Doucet S, Soussignan R, Sagot P. et al. The secretion of areolar (Montgomeryʼs) glands from lactating women elicits selective, unconditional responses in neonates. PLoS One 2009; 4: e7579
  • 23 Schwegler U, Kohlhuber M, Twardella D. et al. Einfluss der Stillbedingungen in den ersten Lebenstagen auf die Dauer des ausschließlichen Stillens. Geburtsh Frauenheilk 2008; 68: 607-614
  • 24 Dos Santos CO, Dolzhenko E, Hodges E. et al. An epigenetic memory of pregnancy in the mouse mammary gland. Cell Rep 2015; 11: 1102-1109
  • 25 Jacobs A, Abou-Dakn M, Becker K. et al. S3-Leitlinie „Therapie entzündlicher Brusterkrankungen in der Stillzeit“, AWMF Leitlinien-Register Nr. 015/071 (Kurzfassung). Geburtsh Frauenheilk 2013; 73: 1-7
  • 26 Hernandez Yenty QM, Jurgens WJ, van Zuijlen PP. et al. Treatment of the benign inverted nipple: a systematic review and recommendations for future therapy. Breast 2016; 29: 82-89
  • 27 Jeong HS, Lee HK. Correction of inverted nipple using subcutaneous turn-over flaps to create a tent suspension-like effect. PLoS One 2015; 10: e0133588