Bone Phenotype is Always Present But Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency

3'-Phosphoadenosine 5'-phosphosulfate synthase 2 (PAPSS2) deficiency is a rare disorder due to biallelic pathogenic variants in the PAPSS2 gene. This disorder was first described in 1998 by Ahmad et al. and Faiyaz ul Haque et al. To date, 79 patients with PAPSS2 deficiency have been report...

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Váldodahkkit: Didem Helvacıoğlu (Dahkki), Tülay Güran (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: Galenos Yayincilik, 2024-03-01T00:00:00Z.
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100 1 0 |a Didem Helvacıoğlu  |e author 
700 1 0 |a Tülay Güran  |e author 
245 0 0 |a Bone Phenotype is Always Present But Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency 
260 |b Galenos Yayincilik,   |c 2024-03-01T00:00:00Z. 
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520 |a 3'-Phosphoadenosine 5'-phosphosulfate synthase 2 (PAPSS2) deficiency is a rare disorder due to biallelic pathogenic variants in the PAPSS2 gene. This disorder was first described in 1998 by Ahmad et al. and Faiyaz ul Haque et al. To date, 79 patients with PAPSS2 deficiency have been reported. The main reported features of these patients are related to bone abnormalities and clinical/biochemical androgen excess. Disproportionate short stature and symptoms associated with spondylar skeletal dysplasia are the most common clinical features that require clinical attention. Androgen excess has been described much less commonly. This review summarizes the currently published clinical, molecular, and biochemical features of patients with PAPSS2 deficiency. 
546 |a EN 
690 |a papss2 
690 |a androgen excess 
690 |a sulfation 
690 |a brachyolmia 
690 |a semd 
690 |a dheas 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Diseases of the endocrine glands. Clinical endocrinology 
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786 0 |n JCRPE, Vol 16, Iss 1, Pp 4-10 (2024) 
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