Cargando…

Developmental delay in congenital hypothyroidism

Detalles Bibliográficos
Autores principales:	Goyal, Chanan, Naqvi, Waqar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The African Field Epidemiology Network 2021
Materias:	Images in Clinical Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077637/ https://www.ncbi.nlm.nih.gov/pubmed/33995772 http://dx.doi.org/10.11604/pamj.2021.38.165.27321

Ejemplares similares

Lordoscoliosis and hyperlordosis in quadriplegic cerebral palsy
por: Goyal, Chanan Vivek, et al.
Publicado: (2020)

Legg-Calve-Perthes disease
por: Goyal, Chanan, et al.
Publicado: (2021)

Bone chip versus myositis ossificans after supracondylar fracture of humerus
por: Goyal, Chanan, et al.
Publicado: (2022)

Monomelic amyotrophy: a rare disease with unusual features (Hirayama disease)
por: Kulkarni, Chaitanya, et al.
Publicado: (2022)

Maxillary defect correction by aesthetics
por: Bhola, Rajiv Dharampal, et al.
Publicado: (2021)

High cholesterol in COVID-19 leading to lung consolidation and bronchiectasis
por: Burhani, Tasneem Sajjad, et al.
Publicado: (2021)

Polydactyly and associated joint dysfunction for left foot: a quintessence case
por: Chitapure, Tajuddin Burhanuddin, et al.
Publicado: (2021)

Chronic osteomyelitis post fracture
por: Wadhokar, Om Chandrakant, et al.
Publicado: (2021)

Inferior glenohumeral dislocation in an elderly
por: Arora, Sakshi Pritam, et al.
Publicado: (2022)

A pre and post radiological image of Supracondylar fracture managed with open reduction and internal fixation
por: Arora, Sakshi Pritam, et al.
Publicado: (2022)

Effectiveness of Early Physiotherapy in an Infant With a High Risk of Developmental Delay
por: Sant, Namrata, et al.
Publicado: (2021)

Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature
por: Goyal, Chanan, et al.
Publicado: (2021)

A Rare and Unusual Case of Trisomy 10p with Terminal 14q Deletion: A Multidisciplinary Approach
por: Goyal, Chanan, et al.
Publicado: (2021)

Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management
por: Goyal, Chanan, et al.
Publicado: (2020)

Virtual Reality-Based Intervention for Enhancing Upper Extremity Function in Children With Hemiplegic Cerebral Palsy: A Literature Review
por: Goyal, Chanan, et al.
Publicado: (2022)

Non-Immersive Virtual Reality as an Intervention for Improving Hand Function and Functional Independence in Children With Unilateral Cerebral Palsy: A Feasibility Study
por: Goyal, Chanan, et al.
Publicado: (2022)

Vacuolated lymphocytes signifying a metabolic disorder in an infant with developmental delay
por: Salama, Rasha, et al.
Publicado: (2015)

An atypical case of febrile infection-related epilepsy syndrome following acute encephalitis: impact of physiotherapy in regaining locomotor abilities in a patient with neuroregression
por: Goyal, Chanan, et al.
Publicado: (2020)

Haptic Feedback-Based Virtual Reality Intervention for a Child With Infantile Hemiplegia: A Case Report
por: Goyal, Chanan, et al.
Publicado: (2022)

Pericardial effusion uncovering underlying hypothyroidism
por: Ponnapalli, Anoosha, et al.
Publicado: (2021)

Massive pericardial effusion caused by hypothyroidism
por: Schmitt, Willian, et al.
Publicado: (2018)

Pituitary hyperplasia secondary to primary hypothyroidism
por: Martinez Quintero, Beatriz, et al.
Publicado: (2020)

Effect of virtual reality and haptic feedback on upper extremity function and functional independence in children with hemiplegic cerebral palsy: a research protocol
por: Goyal, Chanan, et al.
Publicado: (2022)

Evaluation of the developmental outcome in children with congenital hypothyroidism
por: Ehsani, Razieh, et al.
Publicado: (2021)

Pituitary Macroadenoma Secondary to Congenital Hypothyroidism With Growth Failure and Developmental Delay: A Rare Presentation
por: Lohiya, Sham, et al.
Publicado: (2023)

Congenital cataract and congenital glaucoma in Marshall-Smith syndrome
por: Sayadi, Jihene, et al.
Publicado: (2021)

Xia-Gibbs Syndrome: A Review of Literature
por: Goyal, Chanan, et al.
Publicado: (2020)

An Unusual Adult Complex Congenital Heart Disease
por: Lee, Wei-Chieh, et al.
Publicado: (2018)

Congenital bronchial atresia misdiagnosed as pulmonary tuberculosis
por: Panigrahi, MK, et al.
Publicado: (2015)

Bilateral congenital severe microphthalmia in two siblings
por: Sayadi, Jihene, et al.
Publicado: (2022)

Infantile Blount disease: a developmental tibial growth defect
por: Phansopkar, Pratik, et al.
Publicado: (2021)

A Novel Method for Muscle Elongation in Myalgia with Naqvi's-Dynamic Electrical Therapy Approach (DELTA)©: The First-Ever Case Report
por: Naqvi, Waqar M, et al.
Publicado: (2022)

Congenital arteriovenous malformation of upper trunk in a child
por: Singh, Rohan Kumar, et al.
Publicado: (2021)

The congenital melanocytic nevus: a rare clinical image
por: Kumari, Darshana, et al.
Publicado: (2022)

A case of congenital genu recurvatum in a newborn
por: Ramachandran, Umadevi, et al.
Publicado: (2022)

Congenital limbal dermoid in a 10-year-old male
por: Saldanha, Chrisann, et al.
Publicado: (2023)

Congenital mucocele of the tongue: an unusually large presentation without obstruction
por: Choffor-Nchinda, Emmanuel, et al.
Publicado: (2023)

Ataxia and developmental delay as the main manifestation of rhombencephalosynapsis
por: Paktinat, Mohammad, et al.
Publicado: (2018)

A 7-year-old girl with giant congenital biliary dilatation
por: Xu, Xiaolei, et al.
Publicado: (2023)

Congenital clitoromegaly in an adult
por: Touzani, Mohammed Alae, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_o2qcf9jlnkmj77nb281v32gh78