Results 121 to 130 of about 17,278 (220)

Pituitary abscess syndrome in a greater kudu (Tragelaphus strepsiceros)

open access: yesVeterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract An adult male greater kudu (Tragelaphus strepsiceros) presented for a fractured distal left horn. Twelve weeks later, lethargy, pruritus and left periocular swelling were noted. Avulsion of the left horn occurred 1 month later, revealing a necrotic horn base.
Michelle R. Greenfield‐Feig   +4 more
wiley   +1 more source

Multiple congenital anomalies in a neonatal goat kid: Atresia ani, rectovaginal fistula, renal fusion, ectopic ureter and sinus of Valsalva aneurysm

open access: yesVeterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract A 2‐week‐old female Anglo‐Nubian goat kid was presented with rectal malformation and signs of lower urinary and gastrointestinal dysfunction. Postmortem examination revealed multiple congenital anomalies including atresia ani with a rectovaginal fistula, right‐sided extramural ectopic ureter, renal fusion with unilateral severe pallor and ...
Caro Wilson   +3 more
wiley   +1 more source

Diagnosis and management of neutropenia in adults: Expert guidance

open access: yesBritish Journal of Haematology, Volume 209, Issue 2, Page 432-440, August 2026.
Severe neutropenia can result from decreased production of neutrophil precursors in the bone marrow, as in the case of severe congenital neutropenia, or from increased utilization of neutrophils or their accelerated destruction as for drug‐induced neutropenia or autoimmune neutropenia. Severe chronic neutropenia increases susceptibility to bacterial or
Karl Welte   +5 more
wiley   +1 more source

Comprehensive Assessment of the KDM2B‐Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome

open access: yesClinical Genetics, Volume 110, Issue 2, Page 150-164, August 2026.
We set out to characterize genotype–phenotype correlations in the recently delineated KDM2B‐associated neurodevelopmental disorder. We observe a highly penetrant CxxC domain‐related phenotype with distinct facial features supported by GestaltMatcher. In contrast, our findings point to variable expressivity and incomplete penetrance of loss‐of‐function ...
Amber S. E. van Oirsouw   +30 more
wiley   +1 more source

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