患有麦库恩-阿尔布莱特综合征的女孩：案例研究

Q3 Pharmacology, Toxicology and Pharmaceutics

Pharmacognosy Journal Pub Date : 2024-07-01 DOI:10.5530/pj.2024.16.119

Khairunnisa Khairunnisa, Muhammad Faizi, Nur Rochmah,Yuni Hisbiyah, R. Perwitasari

引用次数: 0

摘要

麦库恩-阿尔布莱特综合征（McCune-Albright Syndrome，MAS）是一种罕见的遗传病，其特征是骨骼、皮肤和内分泌系统受累。我们报告了一名 6 岁女孩的病例，她患有纤维状发育不良、咖啡色黄斑、皮肤和内分泌系统受累。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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A Girl with McCune-Albright Syndrome: Case Study

McCune-Albright syndrome (MAS) is a rare genetic disease characterized by skeletal, cutaneous, and endocrine system involvement. We report a 6-year-old girl with fibrous dysplasia, café-au-lait macula

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来源期刊

Pharmacognosy Journal Pharmacology, Toxicology and Pharmaceutics-Pharmacology

CiteScore

2.20

自引率

0.00%

发文量

151

期刊介绍： In 2004, as the PHCOG.NET – a non-profit private organization dedicated to Natural Products Research leading to develop promising drugs. Our main mission is to make information on herbal drug research readily available in different formats to suit the individual needs. Pharmacognosy Journal (Phcog J.) is one of the six journals published by Phcog.Net, Each issue covers different topics in natural product drug discovery, and also publishes manuscripts that describe pharmacognostic investigations, evaluation reports, methods, techniques and applications of all forms of medicinal plant research