Bronchogenic cyst of the neck in a young patient by Yong Li, Keqian Cheng, Na Zheng, Rongguo Wang

Subjects: “…Congenital disorder…”
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Total Anonychia Congenita with Carpal Synostosis by Milad Bahari, Negar Douzandeh

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Cutaneous vascular hamartoma in a lamb by Raissa Morais, Ana Paula Maurique, Janice Villela, Luciana Sonne, Bruno Anjos

Subjects: “…congenital disorder…”
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Bilateral Femoral Duplication and Fibular Agenesis Associated with Bilateral Lower Limb Ectrodactyly: A Rare Case Report by Chetan M, Santosh Reddy Patil, Bharathi M, Vamshi Krishna, Ravi Garg

Subjects: “…congenital disorder…”
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Editorial: Inherited Protein Glycosylation Defects in Humans by Aleksandra Jezela-Stanek, Karolina M. Stepien, Anna Tylki-Szymanska

Subjects: “…congenital disorder of glycosylation…”
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Focal cutaneous telangiectasia in a young dog of probable congenital origin by Akira Ueyama, Tomoya Hoshino, Midori Goto Asakawa, Toshio Shimada, Masahiko Nagata

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Prune belly syndrome: A rare case report by Siddinath Gyawali, Balkrishna Gyawali, Bhumika Ghimire, Bibek Shrestha, Pratima Khanal, Geha Raj Dahal, Dinesh Prasad Koirala

Subjects: “…congenital disorder…”
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Double aortic arch presenting with respiratory disorders by Onur Şen, Ersin Kadiroğulları, Ünal Aydın, Selen Ismihan Onan

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Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation by Veronica Arora, Sunita Bijarnia-Mahay, Samarth Kulshreshtra, Kanika Singh, Ratna Dua Puri, Ishwar Chandar Verma

Subjects: “…Congenital Disorder of Glycosylation…”
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Causes and results of non-cardiac surgeries in newborns admitted to the NICU by Fatemeh Eghbalian, Parastoo Najafi, Azar Pirdehghan

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Expanded Mobius Syndrome by J Gordon Millichap

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Novel insight into FCSK‐congenital disorder of glycosylation through a CRISPR‐generated cell model by Maryam Fazelzadeh Haghighi, Hossein Jafari Khamirani, Jafar Fallahi, Ali Arabi Monfared, Korosh Ashrafi Dehkordi, Seyed Mohammad Bagher Tabei

Subjects: “…congenital disorder of glycosylation…”
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Fibrodysplasia Ossificans Progressive: A Case Report on Rare Musculoskeletal Disorder by Manoj Arya, Rajendra Shakunt, Anoop Raj Singh, Shipra Verma, Vinay Kanaujia

Subjects: “…congenital disorder…”
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PIGO deficiency: palmoplantar keratoderma and novel mutations by Marie-Anne Morren, Jaak Jaeken, Gepke Visser, Isabelle Salles, Chris Van Geet, NIHR BioResource, Ilenia Simeoni, Ernest Turro, Kathleen Freson

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Mannose supplementation in PMM2-CDG by Roman Taday, Julien H. Park, Marianne Grüneberg, Ingrid DuChesne, Janine Reunert, Thorsten Marquardt

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Early escharotomy-like procedure for the prevention of extremity autoamputation in harlequin ichthyosis by Yu-Ying Chu, Mei-Yin Lai, Han-Tsung Liao

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Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients by Hossein Moravej, Ruqaiah Altassan, Jaak Jaeken, Gregory M. Enns, Carolyn Ellaway, Shanti Balasubramaniam, Pascale De Lonlay, David Coman, Saadet Mercimek‐Andrews, Peter Witters, Eva Morava

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PIGO‐CDG: A case study with a new genotype, expansion of the phenotype, literature review, and nosological considerations by Rodrigo Tzovenos Starosta, Nino Kerashvili, Cassandra Pruitt, Matthew J. Schultz, Suzanne W. Boyer, Eva Morava, Maria Laura Duque Lasio, Dorothy K. Grange

Subjects: “…congenital disorder of glycosylation…”
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Phosphomannomutase 2 hyperinsulinemia: Recent advances of genetic pathogenesis, diagnosis, and management by Congli Chen, Yanmei Sang

Subjects: “…congenital disorder of glycosylation…”
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Prenatal Ultrasound Diagnosis of Klippel-trenaunay Syndrome Associated with the Thickened Thigh and Dilated Inferior Vena Cava: A Case Report and Literature Review by Shiyun Peng, MM, Pan Yang, MM, Jinzhou Wan, MM, Siyu Yue, MB, Ling Wang, MB, Xiyue Zhang, MB, Fan Yang, MD

Subjects: “…|klippel-trenaunay syndrome|prenatal ultrasonography|prenatal diagnosis|congenital disorder…”
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