Cargando…

Escobar Syndrome with Monodactyly: A Rare Case Report

Escobar syndrome (nonlethal type of multiple pterygium syndrome) is a very rare genetic disorder. The central manifestations of Escobar syndrome are the presence of multiple pterygia, fixed joint contractures, and characteristic facies. Here, we report a case of Escobar syndrome with additional feat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Karad, Somnath, Ahmad, Imran, Tripathi, Sudhanshu, Ali, Sheikh Sarfraz
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757792/ https://www.ncbi.nlm.nih.gov/pubmed/36530816 http://dx.doi.org/10.4103/jiaps.jiaps_241_21

Ejemplares similares

Anesthesic Management for Escobar Syndrome: Case Report
por: Arpaci, Ayse Hande, et al.
Publicado: (2011)

Airway management in Escobar syndrome: A formidable challenge
por: Mathew, Shaji, et al.
Publicado: (2013)

Escobar syndrome in three male patients of same family
por: Amalnath, Deepak S., et al.
Publicado: (2011)

The Role of Platelet-Rich Plasma in Reducing Pain, Pruritis, and Improving Wound Healing of Skin Graft Donor Site
por: Ali, Sheikh Sarfraz, et al.
Publicado: (2022)

Cardiac anomalies associated with Escobar syndrome: A case report and a review of the literature
por: ALGhasab, Naif Saad, et al.
Publicado: (2021)

Perioperative concerns of a patient with Escobar syndrome for ocular surgery
por: Hussain, Sana Yasmin, et al.
Publicado: (2018)

La familia Escobar: Rescate, edición y catálogo de música sonorense
por: Terán Diáz Landa, María del Rocio
Publicado: (2006)

Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome
por: Najjar, Dorra, et al.
Publicado: (2022)

Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome
por: Kariminejad, Ariana, et al.
Publicado: (2016)

Técnicas prehispánicas del tejido / Alba Guadalupe Mastache de Escobar.
por: Mastache de Escobar, Alba Guadalupe
Publicado: (1971)

Impaired gating of γ‐ and ε‐AChR respectively causes Escobar syndrome and fast‐channel myasthenia
por: Shen, Xin‐Ming, et al.
Publicado: (2023)

Visit of Ambassador Francisca E. Méndez Escobar, Permanent Representative of Mexico to the UNOG
por: Brice, Maximilien
Publicado: (2022)

Ingeniería termodinámica/ M. David Burghardt ; tr., José Carlos Escobar Hernández.
por: Burghardt, M. David
Publicado: (1984)

A rare case of seven siblings with Waardenburg syndrome: a case report
por: Haj Kassem, Luma, et al.
Publicado: (2018)

Angiomyofibroblastoma of the Vulva: A Rare Case Report with Brief Review of Literature
por: Pradhan, Prita, et al.
Publicado: (2019)

Myiasis of open great toe fracture wound: a rare case report
por: Khadka, Sabir K., et al.
Publicado: (2023)

A rare case report: SCARF syndrome
por: Rahimpour, Masoume, et al.
Publicado: (2014)

Case report: Pancytopenia as a rare presentation of Sheehan’s syndrome
por: Rabee’, Hadi, et al.
Publicado: (2022)

Langer-Giedion Syndrome: a Rare Case Report
por: Katge, Farhin Ali, et al.
Publicado: (2016)

Opalski syndrome, a rare variant of wallenberg syndrome, the first case reported from Pakistan: A case report
por: khan, Ubaid, et al.
Publicado: (2023)

Pemphigoid Vegetans in Childhood: A Case Report and Short Review of Literature
por: Khatib, Yasmeen, et al.
Publicado: (2015)

49-years-old women with unusual presentation of severe hypokalemia mimicking Guillain-Barré Syndrome: A rare case report
por: Mohamed, Mohamed Mukhtar, et al.
Publicado: (2022)

Triplication in permanent teeth: A rare case report
por: Gera, Nidhi, et al.
Publicado: (2017)

Colorectal lithobezoar: A rare case report
por: Sheikh, Muzamil Shafi, et al.
Publicado: (2010)

Growing Teratoma Syndrome: A Rare Case Report and Review of the Literature
por: Kampan, Nirmala, et al.
Publicado: (2012)

Bernard Soulier syndrome: A case report from Pakistan
por: Effendi, Iqra, et al.
Publicado: (2023)

Warkany Syndrome: A Rare Case Report
por: Agrawal, Amit, et al.
Publicado: (2011)

Apert's syndrome: Report of a rare case
por: Bhatia, Parul V, et al.
Publicado: (2013)

Kindler's syndrome: A rare case report
por: Suman, Neelam, et al.
Publicado: (2014)

Proteus syndrome: A rare case report
por: Talari, Keerthi, et al.
Publicado: (2012)

Goldenhar Syndrome: A rare case report
por: Bhuyan, Ruchi, et al.
Publicado: (2016)

Crouzon syndrome - A rare case report
por: Kalanjiam, Vidhya, et al.
Publicado: (2017)

Gorlin syndrome: A rare case report
por: Shrivastava, Sandhya, et al.
Publicado: (2020)

Sildenafil: A rare cause of erythema multiforme
por: Sharma, Nidhi Raghunandan, et al.
Publicado: (2016)

A rare case report of a Servelle-Martorell syndrome patient
por: Christanto, Abraham Gita Ramanda, et al.
Publicado: (2023)

Abdominal cocoon syndrome as rare cause of intestinal obstruction: A case report
por: Mousavi, Mir Ali, et al.
Publicado: (2022)

Angiolymphoid Hyperplasia with Eosinophilia Mimicking Multiple Cylindromas: A Rare Case Report
por: Ahmad, Sheikh Manzoor, et al.
Publicado: (2014)

Treatment of generalized pustular psoriasis in pregnancy with systemic corticosteroid: A rare case report
por: Isse Ali, Ahmed, et al.
Publicado: (2022)

Waardenburg-Shah syndrome rare and challenging case report from Somalia
por: Abdi, Abdishakur Mohamed, et al.
Publicado: (2022)

Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report
por: Ali, Syed Yousuf, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_j7pu9lriffncr5s384smbng9lu