Multiple Epiphysäre Dysplasie: 34-jährige ängstlich-depressive Patientin mit positiver Familienanamnese und leichten LWS-Beschwerden

Multiple epiphyseal dysplasia (MED; Fairbank's disease, Ribbin-Muller's disease; ICD 10 F Q78.8) usually occurs autosomal dominant, more rarely also recessive. the prevalence is about 1:20,000 [1, 2]. The development of the epiphyseal plates is disturbed (enchondral ossification). become c...

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Published inPrävention und rehabilitation : Zeitschrift für umfassende Vorbeugung und Behandlung chronischer Krankheiten Vol. 34; no. 1; pp. 37 - 38
Main Authors Koch, H.J., Raschka, C.
Format Journal Article
LanguageEnglish
Published Munich Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG 01.01.2022
Subjects
Case reports
Genetic disorders
Growth disorders
Medical diagnosis
Musculoskeletal diseases
Osteoarthritis
Pain
Pathophysiology
Scoliosis
Spine
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Summary:Multiple epiphyseal dysplasia (MED; Fairbank's disease, Ribbin-Muller's disease; ICD 10 F Q78.8) usually occurs autosomal dominant, more rarely also recessive. the prevalence is about 1:20,000 [1, 2]. The development of the epiphyseal plates is disturbed (enchondral ossification). become clinicala light (Ribbing), mild (Fairbanks) and localized mild form (Meyer). If it occurs in childhood, joint pains are described, especially in the hip and knee joints, occasionally also hand and foot involvement [3]. in the adulthood, the limbs are in often short compared to the trunk. In young osteoarthritic complaints often appear in adulthood. In contrast to the dominant entity is at the recessive shape – very variable courses – the spine is more frequently affected, e.g. mostly mildly pronounced scoliosis and accompanying skeletal changes on [4].
ISSN:0937-552X
DOI:10.5414/PRX0575