Arthrogryposis Multiplex Congenita: Case Report by Ayla Aktulay, Saliha Sağnıç, Özlem Moraloğlu Tekin, Yaprak Engin Üstün, Elif Gül Yapar Eyi, Leyla Mollamahmutoğlu

Subjects: “…Arthrogryposis…”
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Genomic exploration of pediatric neurological disorders: a case series by Naresh Tayade, Gautham Manoj, Akshay Kewat, Anjali Krishna A, Rajiv Devulapalli, Somesh Kumar, Sunil Kumar Polipalli, Bipin G. Nair, Obul Reddy Bandapalli, Prashanth Suravajhala

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VIPAS39 related arthrogryposis-renal dysfunction-cholestasis syndrome—case report and systematic review by Jan Kafol, Barbara Gnidovec Strazisar, Ana Drole Torkar, Matjaz Homan, Sara Bertok, Matej Mlinaric, Jaka Sikonja, Jernej Kovač, Mirjana Perkovic Benedik, Tanja Kersnik Levart, Mojca Zerjav Tansek, Marina Praprotnik, Tadej Battelino, Maruša Debeljak, Urh Groselj

Subjects: “…Arthrogryposis–renal dysfunction–cholestasis syndrome…”
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Identification of novel RIPK4 variants in a Chinese patient with Arthrogryposis Multiplex Congenita (AMC) by Yi-Lei Lu, Meng-wei Liu, Jie-Yuan Jin, Ding Pan

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Unsafe Care and Fake News in Freeman–Burian Syndrome by Mikaela I. Poling, Craig R. Dufresne

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Diagnosis and Management of Freeman-Burian Syndrome: A Case Report by Aidin Arabzadeh, Hossein Azaditalab, Hesam Alitaleshi, Mohammad Reza Abbaszadeh

Subjects: “…Keywords: Craniocarpotarsal dysplasia; Distal arthrogryposis type 2A; Freeman-Burian syndrome; Freeman-Sheldon syndrome; Whistling face syndrome…”
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