Literature DB >> 32476286

A case report of Noonan syndrome-like disorder with loose anagen hair 2 treated with recombinant human growth hormone.

Ping Zhou1,2,3,4,5, Lin Zhu1,2,3,4,5, Qiongli Fan6, Yongfang Liu7, Tianxiu Zhang1,2,3,4,5, Ting Yang2,3,4,5, Jie Chen2,3,4,5, Qian Cheng1,2,3,4,5, Tingyu Li1,2,3,4,5, Li Chen1,2,3,4,5.   

Abstract

Protein phosphatase 1 catalytic subunit beta (PPP1CB) is a disease-causing gene of Noonan-like syndrome, which acts via the RAS/MAPK pathway. To date, only 17 patients diagnosed with PPP1CB-related Noonan-like syndrome have been reported around the world, with few reports in Asia. Twelve reported patients are of short stature and only one patient was treated with growth hormone (GH); however, follow-up data is lacking. To the best of our knowledge, this is the first reported patient with complete recombinant human growth hormone (rhGH) treatment follow-up data; the patient has a de novo c.146C>G (p.Pro49Arg) mutation in the PPP1CB gene. The hair pattern of the patient (coarse, curly, slow growing, and fragile) combined with Noonan dysmorphic features, developmental delay, and congenital heart disease, are highly consistent with the typical features observed in Noonan syndrome-like disorder with loose anagen hair 2 (NSLH2). rhGH treatment, administered for 3 years and 8 months, promoted the patient's linear growth. Our findings expand the data regarding the treatment of short stature in patients with NSLH2 caused by PPP1CB mutation. Clinical manifestation, growth and development process, and rhGH therapy effect data will aid in future revision of the relevant diagnosis and treatment guidelines.
© 2020 Wiley Periodicals LLC.

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Keywords:  zzm321990PPP1CB; Noonan syndrome-like disorder with loose anagen hair 2 (NSLH2); linear growth; recombinant human growth hormone; treatment

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Year:  2020        PMID: 32476286     DOI: 10.1002/ajmg.a.61638

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  1 in total

1.  Case report: Identification and clinical phenotypic analysis of novel mutation of the PPP1CB gene in NSLH2 syndrome.

Authors:  Xuemei He; Xiuli Ma; Jing Wang; Zhuo Zou; Haoyu Huang; Jian Ren; Chunming Liu; Nan Zheng; Jing Ma; Yun Liu
Journal:  Front Behav Neurosci       Date:  2022-09-08       Impact factor: 3.617

  1 in total

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