Results 171 to 180 of about 726,961 (271)
Dermoid cyst associated with segmental multicystic renal dysplasia: A rare case. [PDF]
Laribi S +7 more
europepmc +1 more source
ABSTRACT Aneurysmal bone cyst (ABC) of the radial diaphysis is rare and may mimic telangiectatic osteosarcoma on imaging. We report a young woman with progressively enlarging, painful forearm swelling due to ABC, treated by en bloc resection and fibular strut autograft reconstruction, achieving pain‐free union, good function and no recurrence at short ...
Abdul Hadi Khan +6 more
wiley +1 more source
Long-Term Renal Transplant Success Is Possible in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome: A Case Report. [PDF]
Alvey L +3 more
europepmc +1 more source
ABSTRACT Hepatic AL amyloidosis can cause severe cholestasis independent of marrow tumor burden. In patients with absolute contraindications to high‐dose steroids—such as steroid‐induced psychosis—tailored daratumumab regimens with low‐dose corticosteroids can drive rapid, life‐saving organ reversal.
R. Ceccarelli +8 more
wiley +1 more source
Diagnosing Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome and a Novel GATA3 Variant. [PDF]
Valenciaga A +3 more
europepmc +1 more source
ABSTRACT Autoimmune atrophic gastritis causes loss of oxyntic glands, reduced acid secretion, compensatory hypergastrinemia, and impaired iron and vitamin B12 absorption. A 46‐year‐old woman with minimal gastrointestinal symptoms had fasting serum gastrin > 1800 ng/L, an erythrocyte sedimentation rate of 109 mm/h, hemoglobin 8.2 g/dL, and microcytosis.
Hatem Mousa Taha, Khaled Hatem Taha
wiley +1 more source
Case report: Hypoparathyroidism-sensorineural hearing loss-renal dysplasia without febrile seizures: a novel mutation in the GATA3 gene. [PDF]
Chen H, Zhang Y, Yang X, Li Y.
europepmc +1 more source
ABSTRACT We report an 18‐year‐old female with GATA2 deficiency presenting with a WHIM‐like phenotype, including pancytopenia, monocytopenia, CD19+ B‐cell depletion, sensorineural hearing loss, and cutaneous warts. Subsequent cytogenetic evaluation revealed monosomy 7 and 7q22 deletion, with bone marrow progression to MDS.
Aziz Eghbali +2 more
wiley +1 more source
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. [PDF]
Kim AH +19 more
europepmc +1 more source

