Journal of Pediatric Genetics

Issue 03 · September 2024

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Original Article
167
Ramos-Mejía, R; del Pino, M; Aza-Carmona, M; Abbate, S; Obregon, M G.; Heath, K E.; Fano, V: Novel FLNB Variants in Seven Argentinian Cases with Spondylocarpotarsal Synostosis Syndrome

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175
Al Balushi, Aaisha; Al Hinai, Mariya; Al Hosni, Alya; Al Amrani, Fatima; Al Maimani, Ashwaq; Al Maki, Nabil; Al Hashmi, Nadia: Distal Arthrogryposis with Impaired Proprioception and Touch: A Novel Variant in PIEZO2 Gene in Omani Patients and a Genotype–Phenotype Review from a Single-Center Experience

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181
Wacharasindhu, Suttipong; Ittiwut, Chupong; Ittiwut, Rungnapa; Aroonparkmongkol, Suphab; Suphapeetiporn, Kanya: A Novel NR5A1 Mutation in a Thai Boy with 46, XY DSD

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185
J., Shantala; Upadhyay, Zalak; N., Vani H.; Sathyanarayana, Santhosh Olety; Palany, Raghupathy; J., Shruthi: Clinical Experience from a Single Tertiary Care Center: Neonatal Diabetes Mellitus with Multiple Epiphyseal Dysplasia—Wolcott–Rallison's Syndrome

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190
Ayaz, Akif; Doğru, Zeynep; Kök, Kıvanç; Bayram, Nihan; Yaman, Yöntem; Köseoğlu, Abdullah Hüseyin; Yiğitbaşı, Türkan; Öztürk Demir, Aslı Güner; Yüksel, Elçin; Dundar, Burcu; Çaralan, Erdal Fırat; Nepesov, Serdar; Elli, Murat: A Novel Autosomal Recessive Candidate Gene Responsible for RASopathy-Like Phenotype and Bone Marrow Failure: RASA3

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Case Report
200
Chidambaram, Aakash Chandran; Sugumar, Kiruthiga; Sundaravel, Selvamanojkumar; Ramamoorthy, Jaikumar Govindaswamy; Bathula, Siddardha; Dutta, Usha R.: Recurrent Skin Ulcers with Facial Dysmorphism and Sinopulmonary Infections: Thinking Beyond Hyper-IgE Syndrome

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Case-Based Review
205
Laochareonsuk, Wison; Osatakul, Seksit; Intusoma, Utcharee; Maneechay, Wanwisa; Sangkhathat, Surasak: A Novel Mutation of ORNT1 Detected in a Hyperornithinemia–Hyperammonemia–Homocitrullinuria Syndrome Child by Clinical Whole-Exome Sequencing Open Access

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Supplementary Material

Supplementary Material
211
Ghawil, Millad; Omar, Nesrin Ben; Doggah, Milad: Homozygous TBCE Gene Mutation c.155-166del in a Libyan Patient with Sanjad-Sakati Syndrome: Same Gene Mutation Responsible in All Arab Ethnic Patients

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215
Abdelrahman, Hanadi A.; Akawi, Nadia; Al-Shamsi, Aisha M.; Al-Gazali, Lihadh; Ali, Bassam R.: Pontocerebellar Hypoplasia Type 9: A New Case with a Novel Mutation and Review of Literature

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Supplementary Material

Supplementary Material
223
Mirza, Nida; Bharadwaj, Ravi; Malhotra, Smita; Sibal, Anupam: Prolonged Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency

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227
Lourembam, Radhapyari; Gupta, Manish Kumar; Sherwani, Poonam; Verma, Prashant Kumar: Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies in a Young Infant: First Case Entity of Casamassima–Morton–Nance Syndrome from Asia

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232
Tan, Khian Aun; Chew, Hui Bein; Yacob, Yusnita; Khoo, Teik Beng: A Common CHAT Gene Mutation of Congenital Myasthenic Syndrome Found in Kadazandusun Children

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237
Jafar, Bedour; Alemayehu, Hanna; Bhat, Ramachandra; Zayek, Michael: Multiple Intestinal Anomalies in a Newborn with 22q11.2 Microdeletion Syndrome: A Case Report and Literature Review

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245
Thakur, Seema; Paliwal, Preeti; Farmania, Rajni; Khandelwal, Vipin; Garg, Vivek: Phosphofurin Acidic Cluster Sorting Protein 1 Syndrome: Insights Gained on the Multisystem Involvement Reviewing Encoded Protein Interactions?

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Retraction Note
250
Çaksen, Hüseyin: Retraction Note: Importance of Religious Coping in Bereaved Parents after the Death of a Child with Genetic Disorder

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251
Çaksen, Hüseyin: Retraction Note: Parents' Supernatural Beliefs on Causes of Birth Defects: A Review from Islamic Perspective

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252
Çaksen, Hüseyin: Retraction Note: A Brief View of The Prophet Ayyub's (Alayhi As-Salam) Disease: Was It Job's Syndrome?

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