scholarly journals Rare skeletal disorders: a multidisciplinary postnatal approach to diagnosis and management

2021 ◽  
Vol 171 (5-6) ◽  
pp. 94-101
Author(s):  
Nina-Katharina Walleczek ◽  
Kristina Förster ◽  
Martina Seyr ◽  
Nadja Kadrnoska ◽  
Jennifer Kolar ◽  
...  

SummarySkeletal disorders are inherited disorders with significant skeletal involvement and most of them are rare or extremely rare. Based on the clinical, radiological and genetic phenotype, the group of skeletal disorder comprises more than 450 different and highly heterogeneous disorders. In skeletal disorders rapid and precise diagnoses are urgently needed for patient care and are based on the combination of clinical, radiological and genetic analysis. Novel genetic techniques have revolutionized diagnostics and have a huge impact on counseling of patients and families. Disease-specific long-term management in a multidisciplinary healthcare team in highly specialized centers is recommended to optimize care for these patients. Here we describe a multidisciplinary postnatal approach for the diagnosis and management of patients and families with rare skeletal disorders at the Vienna Bone and Growth Center. We discuss the value of a multidisciplinary diagnostic and management approach in the postnatal setting and provide a diagnostic flowchart for rare skeletal disorders.

2021 ◽  
Vol 429 ◽  
pp. 118893
Author(s):  
Sonda Kammoun ◽  
Mona Rekik ◽  
Khadija Sonda Moalla ◽  
Takwa Sammouda ◽  
Omar Ayadi ◽  
...  

2021 ◽  
Vol 12 (2) ◽  
pp. 103-105
Author(s):  
Shihanah Mansour Alshammari ◽  
Nermeen Nasser Alrajhi ◽  
Shouq Sulaiman Al-Rumayh ◽  
Mohammed Abdullah Alosaimi ◽  
Renad Mohammed Alsharyuf ◽  
...  

Author(s):  
Lujain Ahmed Faraj ◽  
Kholoud Mohammad Alghamdi ◽  
Eman Mohammed Tayyib ◽  
Asma Mohammed Asiri ◽  
Sara Ali Al-Dhahry ◽  
...  

2020 ◽  
Vol 16 (12) ◽  
pp. 2074-2081
Author(s):  
Peter N. Benotti ◽  
G. Craig Wood ◽  
Jila Kaberi-Otarod ◽  
Christopher D. Still ◽  
Glenn S. Gerhard ◽  
...  

2019 ◽  
Vol 45 (07) ◽  
pp. 685-694 ◽  
Author(s):  
Andrew D. Mumford ◽  
Sarah K. Westbury

AbstractRecent advances in genetic analysis are bringing huge benefits to patients with rare genetic disorders, including those with inherited disorders of platelet number and function. Modern clinical hematological practice now has a range of genetic techniques available to enable the precision diagnosis of inherited platelet disorders (IPDs). There are some features of this disparate group of inherited disorders that present specific challenges to establishing an accurate genetic diagnosis. This review aims to introduce the techniques that are relevant for the genetic diagnosis of IPDs and will discuss the key considerations necessary for their application to the clinic.


Blood ◽  
2014 ◽  
Vol 123 (25) ◽  
pp. 3873-3886 ◽  
Author(s):  
Albertine E. Donker ◽  
Reinier A. P. Raymakers ◽  
L. Thom Vlasveld ◽  
Teus van Barneveld ◽  
Rieneke Terink ◽  
...  

AbstractDuring recent years, our understanding of the pathogenesis of inherited microcytic anemias has gained from the identification of several genes and proteins involved in systemic and cellular iron metabolism and heme syntheses. Numerous case reports illustrate that the implementation of these novel molecular discoveries in clinical practice has increased our understanding of the presentation, diagnosis, and management of these diseases. Integration of these insights into daily clinical practice will reduce delays in establishing a proper diagnosis, invasive and/or costly diagnostic tests, and unnecessary or even detrimental treatments. To assist the clinician, we developed evidence-based multidisciplinary guidelines on the management of rare microcytic anemias due to genetic disorders of iron metabolism and heme synthesis. These genetic disorders may present at all ages, and therefore these guidelines are relevant for pediatricians as well as clinicians who treat adults. This article summarizes these clinical practice guidelines and includes background on pathogenesis, conclusions, and recommendations and a diagnostic flowchart to facilitate using these guidelines in the clinical setting.


2022 ◽  
Vol 11 (1) ◽  
pp. 1-3
Author(s):  
Ahmad Hussain Aldhairyan ◽  
Saeed Saleh Hadhrami Alyami ◽  
Anoud Mubarak Saad Alsaad ◽  
Nawaf Ibrahim Al Shuqayfah ◽  
Najd Awwadh Alotaibi ◽  
...  

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