Results 1 to 10 of about 541 (109)

Pseudoacromegaly-A challenging entity in the endocrine clinic: A systematic review. [PDF]

Clinical Endocrinology, Volume 100, Issue 6, Page 542-557, June 2024.
OBJECTIVE: Pseudoacromegaly encompasses conditions with features of acromegaly/gigantism, but no growth hormone (GH) or insulin-like growth factor-1 (IGF-1) excess.
Korbonits, M, Marques, P, Sapinho, I
core   +3 more sources

Pachydermoperiostosis Masquerading as Acromegaly. [PDF]

Journal of the Endocrine Society, 2017
Context: Acromegaly usually is suspected on clinical grounds. Biochemical confirmation is required to optimize therapy, but there are other differential diagnoses.
Cranston, T, Grossman, AB, Halimova, ZY, Karimova, MM, Korbonits, M, Urmanova, YM   +5 more
core   +5 more sources

Pachydermoperiostosis: a rare mimicker of acromegaly [PDF]

Endocrinology, Diabetes & Metabolism Case Reports, 2017
Pachydermoperiostosis is a very rare osteoarthrodermopathic disorder whose clinical and radiographic presentations may mimic those of acromegaly. In the evaluation of patients with acromegaloid appearances, pachydermoperiostosis should be considered as
Azraai Bahari Nasruddin, Noor Rafhati Adyani Abdullah, Wong Lok Chin Jason   +2 more
core   +4 more sources

Pachydermoperiostosis in childhood [PDF]

Rheumatology, 1997
We report a family with pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) spanning four generations with 10 affected individuals, four of whom are children although pachydermoperiostosis is rare in childhood. In this family, with intermarriage, the inheritance is autosomal recessive and it is possible that there are individuals who are ...
W Dodds, G T Lealman, C P Bennett, G P Sinha, P Curtis, D Haigh   +5 more
openaire   +2 more sources

Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report

Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023
X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Abinash Baniya, Ayam Bhattarai, Bibek Devkota, Saurav Khatiwada, Pramod Kumar Kafle, Achyut Krishna Phuyal, Manoj Shahi   +6 more
wiley   +1 more source

Pseudoacromegaly in pachydermoperiostosis [PDF]

BMJ Case Reports, 2016
A 19-year-old male patient presented with a year-long history of progressive painful enlargement of his hands and feet associated with excessive sweating and greasiness of the face, palms and soles. He also noticed pain over his wrists and ankles without any symptoms suggestive of raised intracranial tension and no recent increase in height.
Rana Bhattacharjee, Partha Pratim Chakraborty, Satinath Mukhopadhyay, Subhankar Chowdhury   +3 more
openaire   +2 more sources

Nosology of genetic skeletal disorders: 2023 revision

American Journal of Medical Genetics Part A, Volume 191, Issue 5, Page 1164-1209, May 2023., 2023
Abstract The “Nosology of genetic skeletal disorders” has undergone its 11th revision and now contains 771 entries associated with 552 genes reflecting advances in molecular delineation of new disorders thanks to advances in DNA sequencing technology.
Sheila Unger, Carlos R. Ferreira, Geert R. Mortier, Houda Ali, Débora R. Bertola, Alistair Calder, Daniel H. Cohn, Valerie Cormier‐Daire, Katta M. Girisha, Christine Hall, Deborah Krakow, Outi Makitie, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Ravi Savarirayan, David Sillence, Marleen Simon, V. Reid Sutton, Matthew L. Warman, Andrea Superti‐Furga   +20 more
wiley   +1 more source

A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis

Clinical Case Reports, Volume 11, Issue 5, May 2023., 2023
Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and clinicians can use.
Faiq I. Gorial, Nabaa Ihsan Awadh, Maryam A. Hamzah   +2 more
wiley   +1 more source

Systematic exploration of eczema‐associated paediatric diseases in a Chinese population of millions: A retrospective observation study

Clinical and Translational Allergy, Volume 13, Issue 5, May 2023., 2023
Abstract Background Eczema is the most common form of dermatitis and also the starting point of atopic march. Although many eczema‐associated allergic and immunologic disorders have been studied, there remains a gap in the systematic quantitative knowledge regarding the relationships between all childhood disorders and eczema.
Huiwen Zheng, Jian Yang, Yuqing Feng, Huilong Duan, Lizhong Du, Qiang Shu, Haomin Li   +6 more
wiley   +1 more source

Complete form of pachydermoperiostosis

Anais Brasileiros de Dermatologia, 2020
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy (PHO) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. Its pathogenesis is uncertain and the diagnosis is based on clinical and radiological data.
Mônica Larissa Padilha Honório, Guilherme Holanda Bezerra, Vivianne Lira da Câmara Costa   +2 more
openaire   +5 more sources