Cargando…

Laron Syndrome: A Tale of Two Siblings

Primary growth hormone (GH) resistance or growth hormone insensitivity syndrome, also called Laron syndrome, is a hereditary disease caused by mutations in the GH receptor or in the post-receptor signaling pathway. This disorder is characterized by postnatal growth failure resembling GH deficiency....

Descripción completa

Detalles Bibliográficos
Autores principales:	Das, Niladri, Tarenia, Silima Subhasnigdha, Saha, Souvik, Gaikwad, Prashant Manohar, Hathi, Deep Kamlesh, Goswami, Soumik, Baidya, Arjun, Sengupta, Nilanjan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Journal of the ASEAN Federation of Endocrine Societies 2023
Materias:	Case Series
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692433/ https://www.ncbi.nlm.nih.gov/pubmed/38045665 http://dx.doi.org/10.15605/jafes.038.02.22

Ejemplares similares

ODP587 A Case of Rathke'S Cleft Cyst Presented With Central Diabetes Insipidus In A Young Female
por: Das, Niladri, et al.
Publicado: (2022)

ODP588 A Rare Case Of Infantile Transient Psuedohypoparathyrodism
por: Hathi, Deep, et al.
Publicado: (2022)

Swyer Syndrome Presenting as Dysgerminoma: A Case Report
por: Tarenia, Silima Subhasnigdha, et al.
Publicado: (2023)

A Case of Elephantiasic Pretibial Myxedema Successfully Treated With Intralesional Triamcinolone Acetate
por: Hathi, Deep, et al.
Publicado: (2022)

A Novel Homozygous CYP19A1 Gene Mutation Causing Aromatase Deficiency
por: Hathi, Deep, et al.
Publicado: (2022)

Transformation of Peripheral Sexual Precocity to Central Sexual Precocity Following Treatment of Granulosa Cell Tumor of the Ovary
por: Gaikwad, Prashant M, et al.
Publicado: (2022)

Myriad Manifestations of 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency—A Tale of Two Infants
por: Hathi, Deep, et al.
Publicado: (2022)

Absence of Vitamin D Deficiency Among Outdoor Workers With Type 2 Diabetes Mellitus in Southern West Bengal, India
por: Goswami, Soumik, et al.
Publicado: (2022)

Erratum: Laron syndrome
Publicado: (2020)

Fanconi's anaemia & Laron syndrome: An enigma
por: Kashyap, Rajesh, et al.
Publicado: (2020)

Toward gene therapy of Laron syndrome
por: Werner, Haim
Publicado: (2022)

Focal Epilepsy in Individuals with Laron Syndrome
por: Goldberg, Lotem, et al.
Publicado: (2022)

Laron syndrome in three female siblings with the development of subclinical hypothyroidism and dyslipidemia in one case: first report of a Syrian family
por: Chreitah, Ahmad, et al.
Publicado: (2021)

Treatment for Infertility in Laron Syndrome: A Case Report
por: Alhazidou, Elena, et al.
Publicado: (2022)

Kindler's Syndrome: A Tale of Two Siblings
por: Handa, Navya, et al.
Publicado: (2016)

Ocular findings in two siblings with Joubert syndrome
por: Makino, Shinji, et al.
Publicado: (2014)

Clinical features and endocrine profile of Laron syndrome in Indian children
por: Phanse-Gupte, Supriya R., et al.
Publicado: (2014)

Brittle cornea syndrome: A tale of three brothers
por: Mandlik, Kunal, et al.
Publicado: (2022)

Generation of a miniature pig disease model for human Laron syndrome
por: Cui, Dan, et al.
Publicado: (2015)

Laron Syndrome Research Paves the Way for New Insights in Oncological Investigation
por: Werner, Haim, et al.
Publicado: (2020)

Marjolin’s Ulcer in Laron Syndrome - an Unexpected Combination: A Case Report
por: de la Paz, EM
Publicado: (2020)

Insulin-like growth factors and aging: lessons from Laron syndrome
por: Werner, Haim, et al.
Publicado: (2023)

A Case Report of Familial Extramammary Paget's Disease in Female Siblings
por: Rutnumnoi, Thanachat, et al.
Publicado: (2021)

Too short and too poor: A tale of two siblings
por: Balaji, Laxminarasimhan, et al.
Publicado: (2012)

A tale of four valves: outcome of Brucella endocarditis: a case series
por: Kulkarni, Suraj Kumar, et al.
Publicado: (2019)

Crusted scabies at a tertiary care center: Case series and cautionary tale
por: Lause, Michael, et al.
Publicado: (2023)

Effectiveness and safety of rhIGF1 therapy in patients with or without Laron syndrome
por: Bang, Peter, et al.
Publicado: (2020)

Hemoperitoneum After Cardiopulmonary Resuscitation in Peritoneal Dialysis Patients: A Tale of Two Cases
por: Goel, Narender, et al.
Publicado: (2020)

Choroidal neovascularization secondary to Best’s vitelliform macular dystrophy in two siblings of a Malay family
por: Alisa-Victoria, Koh, et al.
Publicado: (2014)

Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report
por: Cotta, Oana R, et al.
Publicado: (2011)

Genome-Wide Profiling of Laron Syndrome Patients Identifies Novel Cancer Protection Pathways
por: Werner, Haim, et al.
Publicado: (2019)

MON-LB018 Depot-Specific Differences in Adipose Tissue Morphology with Laron Syndrome
por: Geitgey, Delaney, et al.
Publicado: (2019)

False-positive rapid diagnostic test for malaria in new world cutaneous leishmaniasis: a tale of two travelers
por: Unterborn, Rebecca, et al.
Publicado: (2022)

Familial glioblastoma clustering in adult patients: a case report of two non-twin siblings and review of the literature
por: Sander, Caroline, et al.
Publicado: (2019)

Polyembolokoilamania with obsessive compulsive and related disorders: A case series
por: Layek, Avik Kumar, et al.
Publicado: (2023)

Growth Hormone insensitivity (Laron syndrome): Report of a new family and review of Brazilian patients
por: Villela, Thais R., et al.
Publicado: (2020)

Covid-19-related health literacy: a cross-sectional study in Israel: Michal Laron
por: Abdel-Rahman, N, et al.
Publicado: (2022)

Effects of GHR Deficiency and Juvenile Hypoglycemia on Immune Cells of a Porcine Model for Laron Syndrome
por: Schilloks, Marie-Christin, et al.
Publicado: (2023)

MicroRNA 132-3p Is Upregulated in Laron Syndrome Patients and Controls Longevity Gene Expression
por: Yaron-Saminsky, Danielle, et al.
Publicado: (2021)

Identification and In Vitro Functional Verification of Two Novel Mutations of GHR Gene in the Chinese Children with Laron Syndrome
por: Li, Ran, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_k0hrr3gg3h170l40k5f8k3f4bp