A Case Report of Dextrocardia with Situs Inversus: A Rare Condition and Its Clinical Importance von Deshimo, Girma, Abebe, Haile, Damtew, Getiye, Demeke, Enguday, Feleke, Seife

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A Young Woman with Common Variable Immunodeficiency: The Role of Thorough Medical History and Physical Examination in Accurate Diagnosis von Khodadadi, Amirhossein, Khodashahi, Rozita

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Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations von Nishimura, Gen, Dai, Jin, Lausch, Ekkehart, Unger, Sheila, Megarbané, André, Kitoh, Hiroshi, Kim, Ok Hwa, Cho, Tae-Joon, Bedeschi, Francesca, Benedicenti, Francesco, Mendoza-Londono, Roberto, Silengo, Margherita, Schmidt-Rimpler, Maren, Spranger, Jurgen, Zabel, Bernhard, Ikegawa, Shiro, Superti-Furga, Andrea

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Delayed Diagnosis of Perrault Syndrome: A Rare Genetic Disorder von Bayanova, Mirgul, Abilova, Aigerim, Nauryzbayeva, Alisa, Turarbekova, Zhibek

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Case of T-B+NK+ X-Linked Severe Combined Immunodeficiency Disease von Qian, Wenya, Wu, Min, Wang, Guanling

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Dravet Syndrome: A Rare Form of Epilepsy von Hosani, Salwa Al, Varghese, Sona

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DNAH11 and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the Literature von Sodeifian, Fatemeh, Samieefar, Noosha, Shahkarami, Sepideh, Rayzan, Elham, Seyedpour, Simin, Rohlfs, Meino, Klein, Christoph, Babaie, Delara, Rezaei, Nima

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Antithrombin Deficiency Is Associated with a Novel Homozygous Detrimental Mutation in SERPINC1 Gene in a Saudi Female von Alqarni, Sana, Alqarni, Baraah, Alsultan, Abdulrahman

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Hallermann–Streiff Syndrome and Lower Limb Lymphedema with Nasal Obstruction von Pereira de Godoy, Ana Carolina, Pereira de Godoy, Henrique Jose, Pereira de Godoy, Jose Maria

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Acute Pancreatitis in Individuals with COVID-19: A Case Report and Critical Review of Literature von Jamali, Arsia, Nemovi, Khashayar, Bayraktutar, Betul N., Farzaneh, Adam, Chan, Kevin, Ramirez, Carlos, Shahkamrani, Elika, Perumbeti, Anil

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Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome von Mégarbané, Hala, Mégarbané, André

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Mild Late-Onset Sensory Neuropathy Associated with Heterozygous Missense GDAP1 Variants von Jerath, Nivedita U.

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Primary Multifocal Recurrent Urinary Bladder Amyloidosis: A Rare Case Report from Syria von Doya, Leen Jamel, Doya, Lama, Al-Yousef, Khaled, Adib, Ali, Al Shamali, Abedallah, Al Deeb, Basel, Kanan, Mohamad

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15q Duplication Syndrome: Report on the First Patient from Ecuador with an Unusual Clinical Presentation von Ortiz-Prado, Esteban, Iturralde, Ana Lucía, Simbaña-Rivera, Katherine, Gómez-Barreno, Lenin, Hidalgo, Iván, Rubio-Neira, Mario, Espinosa, Nicolás, Izquierdo-Condoy, Juan, Arteaga-Espinosa, María Emilia, Lister, Alex, López-Cortés, Andrés, Cabrera-Andrade, Alejandro

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Dengue Infection and Its Relationship with Evans Syndrome: A Pediatric Case von Ardila Gomez, Ivan Jose, López, Pilar Pérez, Hernández Carreño, Mónika Rocío, Barrios Torres, Juan Camilo

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Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men von Auguste, Yasmina, Delague, Valérie, Desvignes, Jean-Pierre, Longepied, Guy, Gnisci, Audrey, Besnier, Pierre, Levy, Nicolas, Beroud, Christophe, Megarbane, André, Metzler-Guillemain, Catherine, Mitchell, Michael J.

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Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H) von Baudot, Cécile, Esteve, Clothilde, Castro, Christel, Poitelon, Yannick, Mas, Camille, Hamadouche, Tarik, El-Rajab, Maryam, Lévy, Nicolas, Megarbané, André, Delague, Valérie

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May–Thurner Syndrome: A Consideration for Deep Vein Thrombosis in Males von Sachdeva, Pooja, Choke, Tieng Chek Edward, Jia Sheng, Tay, Tian En Jason, Tay

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Cough Radiculopathy: Postinfectious Cough-Related Acute Lumbar Radiculopathy von Alkhuja, Samer

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Sclerotic Bone Metastasis in Pulmonary Adenocarcinoma von Mohammed, Riyadh Ali, Ghadban, Wisam, Farooqui, Khalid

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