Cargando…

Sanjad-Sakati Syndrome Dental Management: A Case Report

Sanjad-Sakati syndrome (SSS) is a rare genetic disorder with autosomal recessive pattern of inheritance characterized by hypoparathyroidism, sever growth failure, mental retardation, susceptibility to chest infection, and dentofacial anomalies. A child with SSS was referred to the dental departments...

Descripción completa

Detalles Bibliográficos
Autor principal:	El Batawi, Hisham Y.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600134/ https://www.ncbi.nlm.nih.gov/pubmed/23533822 http://dx.doi.org/10.1155/2013/184084

Ejemplares similares

Dental Management of a Tunisian Child with Sanjad-Sakati Syndrome
por: Chouchene, Farah, et al.
Publicado: (2022)

Anesthetic management of a case of Sanjad-Sakati syndrome
por: Alshoaiby, AN, et al.
Publicado: (2016)

Endocrinological Manifestations of Sanjad-Sakati Syndrome
por: Bashar, Masharib, et al.
Publicado: (2020)

Corneal opacification in Sanjad-Sakati syndrome
por: Elhusseiny, Abdelrahman M., et al.
Publicado: (2022)

Sanjad-Sakati Syndrome and Its Association with Superior Mesenteric Artery Syndrome
por: AlAyed, Osamah Abdullah
Publicado: (2014)

Neurological manifestations in children with Sanjad–Sakati syndrome
por: Elhassanien, Ahmed Farag, et al.
Publicado: (2013)

Oral Facial Manifestations of Sanjad–Sakati Syndrome: A Literature Review
por: Alghamdi, Sara
Publicado: (2022)

The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin
por: Ratbi, Ilham, et al.
Publicado: (2015)

A Staghorn Calcium Phosphate Stone in a Child With Sanjad-Sakati Syndrome: An Iatrogenic Manifestation?
por: Alomar, Mohammad A, et al.
Publicado: (2022)

Correcting hypophosphataemia in a paediatric patient with Sanjad–Sakati syndrome through a single oral dose of potassium phosphate intravenous solution
por: Sabti, Mnaff A, et al.
Publicado: (2021)

Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad–Sakati syndrome()
por: Aminzadeh, Majid, et al.
Publicado: (2018)

SUN-518 Sanjad Sakati Syndrome - A Rare Cause Of Congenital Hypoparathyroidism And Severe Short Stature - A Case Report
por: Boyd, Jennifer, et al.
Publicado: (2019)

The Successful Management of Primary Amenorrhea in Woodhouse–Sakati Syndrome: A Case Report and a Literature Review
por: Bakhsh, Hanadi, et al.
Publicado: (2023)

Minimizing the Risk of Perioperative Bleeding in a Child with Hemophilia A during Dental Rehabilitation under General Anesthesia: A Case Report
por: Yehia El Batawi, Hisham
Publicado: (2013)

Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies
por: Alharbi, Mariam S.
Publicado: (2021)

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
por: Hdiji, Olfa, et al.
Publicado: (2016)

Radiological Findings of Woodhouse-Sakati Syndrome: Cases Reported From Saudi Arabia
por: Alzahrani, Arwa M, et al.
Publicado: (2022)

Three Siblings With Woodhouse-Sakati Syndrome: A Case Report of A New Saudi Family
por: Alhuzaim, Omar N, et al.
Publicado: (2022)

Woodhouse-Sakati Syndrome Presenting With Psychotic Features After Starting Trihexyphenidyl: A Case Report
por: Aljaffer, Mohammed A, et al.
Publicado: (2022)

The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
por: Sheridan, Molly B., et al.
Publicado: (2015)

Effect of preoperative oral midazolam sedation on separation anxiety and emergence delirium among children undergoing dental treatment under general anesthesia
por: El Batawi, Hisham Yehia
Publicado: (2015)

Behavioral management using sequenced treatment paradigm and audiovisual distraction during dental treatment in children with attention deficit/hyperactivity disorder
por: Fakhruddin, Kausar Sadia, et al.
Publicado: (2018)

Patterns of dental caries among school children assessed using Caries Assessment Spectrum and Treatment tool
por: El Batawi, Hisham, et al.
Publicado: (2017)

Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
por: Chen, Guangmin, et al.
Publicado: (2021)

Case Report: Clinical manifestation and dental management of Papillon-Lefèvre syndrome
por: Yousry, Yasmin Mohamed, et al.
Publicado: (2018)

Papillon-Lefèvre Syndrome: Diagnosis, Dental Management, and a Case Report
por: Abou Chedid, Jean-Claude, et al.
Publicado: (2019)

Effectiveness of audiovisual distraction in behavior modification during dental caries assessment and sealant placement in children with autism spectrum disorder
por: Fakhruddin, Kausar Sadia, et al.
Publicado: (2017)

Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review
por: Kohil, Amira, et al.
Publicado: (2023)

Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
por: Zhou, Min, et al.
Publicado: (2021)

Dental management of patient with Williams Syndrome - A case report
por: Wong, Daniel, et al.
Publicado: (2015)

Perceived outcomes and satisfaction of Saudi parents and their children following dental rehabilitation under general anesthesia: A 2-year follow-up
por: El Batawi, Hisham Yehia, et al.
Publicado: (2014)

Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
por: Almeqdadi, Mohammad, et al.
Publicado: (2018)

Dental management of a patient with Moebius syndrome: A case report
por: Chen, Ben, et al.
Publicado: (2021)

Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
por: Zhou, Min, et al.
Publicado: (2022)

Diagnosis and Dental Management of a Child with Moebius Syndrome: A Case Report
por: Mittal, Meenu, et al.
Publicado: (2023)

Novel splicing‐site mutation in DCAF17 gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
por: Fozia, Fozia, et al.
Publicado: (2021)

Effectiveness of audiovisual distraction with computerized delivery of anesthesia during the placement of stainless steel crowns in children with Down syndrome
por: Fakhruddin, Kausar Sadia, et al.
Publicado: (2017)

Diagnostic and Treatment Approach in the Management of Dental Anomalies Associated with Stevens–Johnson Syndrome: A Case Report
por: Katyal, Sakshi, et al.
Publicado: (2021)

A case report on dental management of a toddler with Pachygyria
por: Vignesh Ravindran,, et al.
Publicado: (2017)

Epidermolysis Bullosa, Dental and Anesthetic Management: A Case Report
por: Esfahanizade, Katayoun, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_sbk46g2ebg6r8jk1858g4nh0qj