Samar S Hassan
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Explore the profile of Samar S Hassan including associated specialties, affiliations and a list of published articles.
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5
Citations
11
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Recent Articles
1.
Musa S, Abdullah M, Hassan S, Fauzi L, Babiker O, Ahmed A, et al.
Eur J Endocrinol
. 2025 Mar;
PMID: 40063902
Background: Studies of Primary Adrenal Insufficiency (PAI) in African children are rare but in Sudan, congenital adrenal hyperplasia (CAH) and Triple A syndrome are the most common genetic causes. Differential...
2.
Ismail M, Musa S, Hassan S, Abdullah M
J Med Case Rep
. 2023 Jun;
17(1):244.
PMID: 37264371
Background: Hyaline fibromatosis syndrome is a rare progressive autosomal recessive connective tissue disorder caused by a mutation in the ANTXR2/CMG2 gene. According to its severity, patients may present with skin...
3.
Hassan S, Abdullah M, Trebusak Podkrajsek K, Musa S, Ibrahim A, Babiker O, et al.
Genes (Basel)
. 2022 Apr;
13(4).
PMID: 35456463
Pathogenic variants within the gene encoding the pituitary-specific transcription factor, POU class 1 homeobox 1 (), are associated with combined pituitary hormone deficiency (CPHD), including growth hormone, prolactin, and thyrotropin...
4.
Musa S, Hassan S, Ahmed A, Ngwiri T, Fadlalbari G, Ibrahim A, et al.
J Pediatr Endocrinol Metab
. 2021 Oct;
35(2):231-237.
PMID: 34653327
Objectives: Primary adrenal insufficiency (PAI) in children is an uncommon condition. Congenital adrenal hyperplasia (CAH) is the commonest cause followed by autoimmune disorders. Diagnosis and management are challenging especially in...
5.
Hassan S, Mukhwana R, Musa S, Ibrahim A, Babiker O, Abdullah M
Sudan J Paediatr
. 2021 Apr;
21(1):53-60.
PMID: 33879944
There is paucity of reported information regarding aetiology and clinical profile of hypopituitarism from resource-limited countries particularly in populations with high rates of consanguineous marriages. Here, we are reporting the...
6.
Musa S, Ibrahim A, Hassan S, Johnson M, Basheer A, Arabi A, et al.
Int J Pediatr Endocrinol
. 2020 Dec;
2020(1):21.
PMID: 33292488
Background: Fanconi-Bickel syndrome (FBS) is a rare condition of carbohydrate metabolism, caused by a recessive defect in the facilitative glucose transporter GLUT2 encoded by the SLC2A2 gene and characterized by...