Frontonasal dysplasia Sequence : A case report by Bello M, Garandawa H, Mustapha Z, Isa A, Tahir C, Ngamdu YB, Machoko Y, Abubakar H, Djossi SK

Subjects: “…dysmorphism…”
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Crouzon syndrome and the eye: An overview by Kasturi Bhattacharjee, Obaidur Rehman, Vatsalya Venkatraman, Don Kikkawa, Harsha Bhattacharjee, Rahul Gogoi, Aditi Mehta Grewal, Pragya Bhattacharjee

Subjects: “…craniofacial dysmorphism…”
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An infant with 49XXXXY syndrome: a case report by N. P. G. C. R. Naotunna, C. Liyanage, N. Atapattu

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Prevalence and effect of body dysmorphic disorder in females at Madinah, Saudi Arabia by Asma M AlOtaibi, Mansour M Almuzaini, Mzoun A Alotaibi, Razan M Alotaibi

Subjects: “…body dysmorphism…”
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Identification of a heterozygous ACAN mutation in a 15-year-old boy with short stature who presented with advanced bone age: a case report and review of the literature by Tae Youp Kim, Kyung Mi Jang, Chang Won Keum, Seung Hwan Oh, Woo Yeong Chung

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Holoprosencephaly Variant by J Gordon Millichap

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Cherubism: a rare case report with literature review by A. Lahfidi, MD, W.M. Traore, MD, I.D. Diallo, MD, N. Lrhorfi, MD, S. Elhaddad, MD, N. Allali, MD, L. Chat, MD

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Bilateral proptosis in Marshall-Smith syndrome by Deepsekhar Das, Divya Chauhan, Sahil Agrawal, Mandeep Singh Bajaj

Subjects: “…craniofacial dysmorphism…”
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Blastocyst Morphology Holds Clues Concerning The Chromosomal Status of The Embryo by Rita de Cassia Savio Figueira, Amanda Souza Setti, Daniela Paes Almeida Ferreira Braga, Assumpto Iaconelli Jr., Edson Borges Jr.

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Congenital Arthrogryposis and Maternal Myasthenia by J Gordon Millichap

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Case report of 49, XXXXY syndrome: first case in Oman by Musallam Said Al Araimi, Salwa Ali AlObaidani, Zainab Al Hashmi, Ruba Al Lawati, Hiba Al Mazrooai Al Mazrooai

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Three Siblings with Cohen Syndrome and a Novel Vacuolar Protein Sorting 13 Homolog B Mutation by Naseer Yousuf Mir, Altaf Hussain, Khurshid Ahmad Wani, Sanjeet Singh, Ummar M Bhat

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The promise of the metaverse in mental health: the new era of MEDverse by Antonio Cerasa, Andrea Gaggioli, Flavia Marino, Giuseppe Riva, Giovanni Pioggia

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Case report: A Chinese boy with facial dysmorphism, immunodeficiency, livedo, and short stature syndrome by Lihong Jiang, Xin Chen, Jiaqi Zheng, Meilin Wang, Hui Bo, Hui Bo, Geli Liu

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[PROVISIONAL] Non-mosaic partial duplication 12p in a patient with dysmorphic characteristics and developmental delay by Jakeline Santos Oliveira, Tatiana Mozer Joaquim, Rosana Aparecida Bicudo da Silva, Deise Helena de Souza, Lúcia Regina Martelli, Danilo Moretti-Ferreira

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Myelomonocytic leukaemia (JMML) in a child with intellectual disability and chromosome 4q deletion by Harsha Prasada Lashkari, Naga Venkata Sirisha Andey, Nanda Kumar, Katta M. Girisha

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Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS) by Xianru Jiao, Jiao Xue, Pan Gong, Xinhua Bao, Ye Wu, Yuehua Zhang, Yuwu Jiang, Zhixian Yang

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Chromosome 1p31.1 deletion syndrome: Limited expression by Seba Biswal, Preetinanda Parida, Aranya Dubbudu, Indar Kumar Sharawat, Prateek Kumar Panda

Subjects: “…facial dysmorphism…”
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Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism by Abdulaziz Alsemari, Banan Al-Younes, Ewa Goljan, Dyala Jaroudi, Faisal BinHumaid, Brian F. Meyer, Stefan T. Arold, Dorota Monies

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Myhre syndrome: the first case in Korea by Dongjin Lim, Jae Hyun Kim, Jieun Lee

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