Results 51 to 60 of about 14,669 (176)
PHACE(S) syndrome: Report of a case with new ocular and systemic manifestations
Journal of Current Ophthalmology, 2017 Purpose: To describe an infant with PHACE(S) syndrome [posterior fossa anomalies (P), hemangiomas (H), arterial anomalies (A), cardiac abnormalities and coarctation of aorta (C), eye abnormalities (E), and the sternal defects (S)] with unusual strabismus,
Raheleh Assari +4 more
doaj +1 more source
Microspherophakia in a 47, XYY Syndrome Patient: A Case Report
Case Reports in Ophthalmology, 2020 47, XYY syndrome affects males with variable phenotypic expression. Around 80–99% of affected individuals present low-set ears, malar flattening, motor delay, and tall stature. Yet, some cases lack signs or symptoms or are barely noticeable.
Maria Lourdes Rubalcava-Soberanis +4 more
doaj +1 more source
Клінічний випадок morning glory syndrome
Archive of Ophthalmology and Maxillofacial Surgery of UkraineАктуальність. Рідкісна вроджена патологія, синдром в’юнка, або синдром ранкового сяйва (англ. morning glory syndrome), є лійкоподібною екскавацією заднього полюса очного яблука із залученням диска зорового нерва.
Л.В. Венгер +5 more
semanticscholar +1 more source
New Phytologist, Volume 250, Issue 2, Page 762-787, April 2026.Summary B‐box (BBX) proteins were initially characterized as transcription factors connecting light signaling to the regulation of flowering time and seedling photomorphogenesis. However, over the last decade, increasing evidence has shown that they integrate light and hormone signaling, modulating multiple physiological processes during plant life. In
Bruno Silvestre Lira +3 more
wiley +1 more source
African Decolonial Theory: A Conversation
Antipode, Volume 58, Issue 2, March 2026.Abstract Antipode has become a key platform for engaging with decolonial and anticolonial scholarship, as well as adjacent fields such as Black geographies, Indigenous studies, Latin American feminism, and work on settler‐colonialism. African reference points in this literature, however, have been far less common, both in the journal and more broadly ...
Patricia Daley +10 more
wiley +1 more source
Diagnostic Pathology, 2023 Germ cell tumours with somatic-type solid malignancy (GCT-STM) are a rare disease of the mediastinum. Recently, a cohort of vasculogenic mesenchymal tumour (VMT)-nonseminoma cases with different prognoses were recognized and reported.
Shang Zhanxian +3 more
doaj +1 more source
International Journal of Clinical Practice, Volume 2026, Issue 1, 2026.Parkinson’s disease (PD) and atypical parkinsonian syndromes (APSs) present diagnostic challenges due to overlapping clinical features. Misdiagnosis rates exceed 25% for PD and 50% for APS, highlighting the need for improved diagnostic methods. To review current diagnostic approaches and explore the potential of plasma biomarkers in differentiating PD ...
Fatuma Mohamed Aden +8 more
wiley +1 more source
Journal of Obesity, Volume 2026, Issue 1, 2026.Background Obesity is a chronic, multifactorial disease associated with significant cardiometabolic, psychological, and socioeconomic consequences. Its complex etiology necessitates integrated, evidence‐based management strategies beyond simple caloric restriction.
Iman Saad Ahmed +7 more
wiley +1 more source
Case Reports in Ophthalmological Medicine, 2018 Turner syndrome is a common sex chromosome disorder affecting females. The disorder is caused by a partial loss, complete absence, or structural abnormality of one X chromosome.
Dev R. Sahni +4 more
doaj +1 more source
Morning glory disc anomaly and facial hemangiomas in a girl with moyamoya syndrome
Indian Journal of Ophthalmology, 2018 Moyamoya disease (MMD) is a chronic progressive, occlusive cerebrovascular disease in the circle of Willis and the feeding arteries. Morning glory disc anomaly (MGDA) is characterized by an abnormal excavated optic disc with radial emergence of blood ...
Sanitha Sathyan, Mariea Chackochan
doaj +1 more source