Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns
Hereditary angioedema (HAE) is a genetically caused orphan disease with a high risk of developing life-threatening attacks, thus requiring availability for up-to-date information on this problem for the doctors of any specialties. A limited number of observations determine the value of the analysis...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | Russian |
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St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists
2020-05-01
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| Series: | Медицинская иммунология |
| Subjects: | |
| Online Access: | https://www.mimmun.ru/mimmun/article/view/1930 |
| _version_ | 1826534170131693568 |
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| author | E. N. Bobrikova A. R. Denisova T. S. Kotomina S. A. Serdotetskova D. S. Fomina |
| author_facet | E. N. Bobrikova A. R. Denisova T. S. Kotomina S. A. Serdotetskova D. S. Fomina |
| author_sort | E. N. Bobrikova |
| collection | DOAJ |
| description | Hereditary angioedema (HAE) is a genetically caused orphan disease with a high risk of developing life-threatening attacks, thus requiring availability for up-to-date information on this problem for the doctors of any specialties. A limited number of observations determine the value of the analysis for each clinical case. Many facets of clinical manifestations, a list of predisposing and triggering factors, as well as limitations of some diagnostic and therapeutic algorithms, require the development of individual management schemes under distinct clinical situations. In this paper, we present the unique clinical cases with certain limitations, describing unexpected onset of the disease in the course of pregnancy, management aspects during delivery and post-delivery periods in a women with a previously confirmed HAE diagnosis. Adapted diagnostic algorithms of postnatal diagnostic verification are presented for children with burdened genetic history. We express some assumptions about involvement of a multidisciplinary team of specialists, personalized approach to building a management plan with an “online” correction depending on observation stage of НАЕ patient. |
| first_indexed | 2024-03-08T05:48:16Z |
| format | Article |
| id | doaj.art-f20019f670644bdcb0ca9fc2dd266123 |
| institution | Directory Open Access Journal |
| issn | 1563-0625 2313-741X |
| language | Russian |
| last_indexed | 2025-03-14T02:18:46Z |
| publishDate | 2020-05-01 |
| publisher | St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists |
| record_format | Article |
| series | Медицинская иммунология |
| spelling | doaj.art-f20019f670644bdcb0ca9fc2dd2661232025-03-11T17:59:11ZrusSt. Petersburg branch of the Russian Association of Allergologists and Clinical ImmunologistsМедицинская иммунология1563-06252313-741X2020-05-0122357758410.15789/1563-0625-SOI-19301292Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newbornsE. N. Bobrikova0A. R. Denisova1T. S. Kotomina2S. A. Serdotetskova3D. S. Fomina4Сlinical Hospital No. 52First Moscow State I. Sechenov Medical UniversityСlinical Hospital No. 52Сlinical Hospital No. 52Сlinical Hospital No. 52; First Moscow State I. Sechenov Medical UniversityHereditary angioedema (HAE) is a genetically caused orphan disease with a high risk of developing life-threatening attacks, thus requiring availability for up-to-date information on this problem for the doctors of any specialties. A limited number of observations determine the value of the analysis for each clinical case. Many facets of clinical manifestations, a list of predisposing and triggering factors, as well as limitations of some diagnostic and therapeutic algorithms, require the development of individual management schemes under distinct clinical situations. In this paper, we present the unique clinical cases with certain limitations, describing unexpected onset of the disease in the course of pregnancy, management aspects during delivery and post-delivery periods in a women with a previously confirmed HAE diagnosis. Adapted diagnostic algorithms of postnatal diagnostic verification are presented for children with burdened genetic history. We express some assumptions about involvement of a multidisciplinary team of specialists, personalized approach to building a management plan with an “online” correction depending on observation stage of НАЕ patient.https://www.mimmun.ru/mimmun/article/view/1930angioedemahereditarypregnancybreastfeedingnewbornschildren |
| spellingShingle | E. N. Bobrikova A. R. Denisova T. S. Kotomina S. A. Serdotetskova D. S. Fomina Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns Медицинская иммунология angioedema hereditary pregnancy breastfeeding newborns children |
| title | Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
| title_full | Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
| title_fullStr | Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
| title_full_unstemmed | Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
| title_short | Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns |
| title_sort | significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation and in newborns |
| topic | angioedema hereditary pregnancy breastfeeding newborns children |
| url | https://www.mimmun.ru/mimmun/article/view/1930 |
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