<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Khairunnisa, Muhammad Faizi</style></author><author><style face="normal" font="default" size="100%">Nur Rochmah</style></author><author><style face="normal" font="default" size="100%">Yuni Hisbiyah</style></author><author><style face="normal" font="default" size="100%">Rayi Kurnia Perwitasari</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Girl with McCune-Albright Syndrome: Case Study</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">June 2024</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">16</style></volume><pages><style face="normal" font="default" size="100%">706-710</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;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, and multiple hyperfunctional endocrinopathies. Treatment was palliative, the patient was planned for surgery on bilateral femur fractures and a rehabilitation program.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Case Report</style></work-type><section><style face="normal" font="default" size="100%">706</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Khairunnisa, Muhammad Faizi*, Nur Rochmah,Yuni Hisbiyah, Rayi Kurnia Perwitasari&lt;/strong&gt;&lt;/p&gt;

&lt;p&gt;Department of Child Health, Faculty of Medicine, Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, INDONESIA.&lt;/p&gt;
</style></auth-address></record></records></xml>