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评估一个具有新型 TBX19 基因突变的儿童的生长和青春期,并回顾文献。

Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature.

机构信息

Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.

Department of Medical Genetics, Bezmialem Vakıf University School of Medicine, Istanbul, Turkey.

出版信息

Hormones (Athens). 2019 Jun;18(2):229-236. doi: 10.1007/s42000-019-00096-7. Epub 2019 Feb 12.

Abstract

BACKGROUND

Biallelic mutations in the TBX19 gene cause severe early-onset adrenal failure due to isolated ACTH deficiency (IAD). This rare disease is characterized by low plasma ACTH and cortisol levels, with normal secretion of other pituitary hormones. Herein, we report a patient with IAD due to a novel TBX19 gene mutation, who is also of tall stature.

CASE REPORT

A 4-year-old girl was presented with loss of consciousness due to hypoglycemia. The patient was born at term with a birth weight of 3800 g. Her parents were first-degree cousins. She had a history of several hospitalizations for recurrent seizures, abdominal pain, and vomiting. At presentation, her weight and height were + 1.8 and + 2.2 SDS, respectively. Serum glucose was 25 mg/dl (1.4 mmol/L), with normal sodium, potassium, and insulin concentrations. The child was hypocortisolemic (0.1 μg/dl), and ACTH levels were extremely low (< 5.0 pg/ml). A diagnosis of IAD was made and hydrocortisone treatment was started. Hypoglycemic episodes, seizures, and recurrent gastrointestinal complaints disappeared after hydrocortisone replacement. Magnetic resonance imaging of the pituitary was normal. Whole exome sequencing revealed a novel homozygous c.302G > A (W101*) mutation in the TBX19 gene.

CONCLUSION

We report a new mutation in the TBX19 gene in a patient with isolated ACTH deficiency. While overgrowth is a known feature of some types of adrenal insufficiencies, including MC2R gene defects and POMC deficiency, it may be a novel feature for TPIT deficiency, as in our patient.

摘要

背景

TBX19 基因的双等位基因突变导致由于 ACTH 缺乏引起的严重早发性肾上腺功能衰竭(IAD)。这种罕见疾病的特征是血浆 ACTH 和皮质醇水平低,其他垂体激素分泌正常。本文报告了一例由于 TBX19 基因突变引起的 IAD 患者,该患者也身材高大。

病例报告

一名 4 岁女孩因低血糖导致意识丧失就诊。患儿足月出生,出生体重 3800 g。其父母为表亲。她曾因反复癫痫发作、腹痛和呕吐多次住院治疗。就诊时,她的体重和身高分别为+1.8 和+2.2 SDS。血清葡萄糖为 25 mg/dl(1.4 mmol/L),钠、钾和胰岛素浓度正常。患儿皮质醇水平低(0.1 μg/dl),ACTH 水平极低(<5.0 pg/ml)。诊断为 IAD,并开始给予氢化可的松治疗。氢化可的松替代治疗后,低血糖发作、癫痫发作和反复胃肠道主诉消失。垂体磁共振成像正常。全外显子组测序显示 TBX19 基因的一个新的纯合 c.302G>A(W101*)突变。

结论

我们报告了一名孤立性 ACTH 缺乏症患者中 TBX19 基因的新突变。虽然过度生长是某些类型肾上腺功能不全(包括 MC2R 基因突变和 POMC 缺乏)的已知特征,但它可能是我们患者中 TPIT 缺乏症的一个新特征。

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