[et_pb_section fb_built=”1″ custom_padding_last_edited=”on|phone” admin_label=”Title Section” _builder_version=”4.19.5″ _module_preset=”default” background_enable_color=”off” use_background_color_gradient=”on” background_color_gradient_stops=”rgba(13,75,126,0.95) 0%|rgba(13,75,126,0.95) 100%” background_color_gradient_overlays_image=”on” background_image=”https:\/\/chungjansensyndrome.eu\/wp-content\/uploads\/2023\/02\/dna-1811955_1920.jpg” custom_margin=”-200px||||false|false” custom_padding=”250px||||false|false” custom_padding_tablet=”250px||||false|false” custom_padding_phone=”190px||0px||false|false” global_colors_info=”{}”][et_pb_row _builder_version=”4.19.5″ _module_preset=”default” custom_padding=”||||false|false” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.19.5″ _module_preset=”default” custom_padding=”|||0px|false|false” global_colors_info=”{}”][et_pb_text admin_label=”Chung-Jansen Syndrome Title” _builder_version=”4.20.2″ text_font=”||||||||” header_font=”Montserrat|700|||||||” header_text_align=”center” header_text_color=”#f7f7f7″ header_font_size=”60px” header_line_height=”1.3em” custom_margin=”||||false|false” header_font_size_tablet=”60px” header_font_size_phone=”30px” header_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n
[\/et_pb_text][et_pb_text disabled_on=”off|on|on” admin_label=”Mobile- What is Chung-Jansen Syndrome?” _builder_version=”4.20.2″ text_font=”Montserrat|500||on|||||” text_text_color=”#353740″ text_font_size=”16px” text_letter_spacing=”3px” header_text_align=”center” header_2_text_align=”center” header_2_text_color=”#f7f7f7″ custom_margin=”||||false|false” animation_direction=”bottom” header_2_font_size_tablet=”” header_2_font_size_phone=”14px” header_2_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n
[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ custom_padding_last_edited=”off|desktop” disabled_on=”on|off|off” admin_label=”Text Overlap Section” _builder_version=”4.20.2″ _module_preset=”default” background_enable_color=”off” background_enable_image=”off” width=”80%” max_width=”1080px” module_alignment=”center” custom_margin=”-50px||||false|false” custom_padding=”||||false|false” custom_padding_tablet=”||||false|false” custom_padding_phone=”20px||20px||false|false” box_shadow_style=”preset1″ global_colors_info=”{}”][et_pb_row use_custom_gutter=”on” gutter_width=”2″ make_equal=”on” _builder_version=”4.20.2″ _module_preset=”default” background_color=”#FFFFFF” custom_margin=”0px||0px||false|false” custom_padding=”0px|0px|0px|0px|false|false” custom_css_main_element=”z-index:1000″ global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.19.5″ _module_preset=”default” background_color=”#FFFFFF” custom_padding=”|0px|||false|false” global_colors_info=”{}”][et_pb_text admin_label=”What is Chung-Jansen Syndrome?” _builder_version=”4.20.2″ text_font=”Montserrat|500||on|||||” text_text_color=”#353740″ text_font_size=”16px” text_letter_spacing=”3px” header_text_align=”center” header_2_text_align=”center” custom_margin=”||||false|false” animation_direction=”bottom” header_2_font_size_phone=”18px” header_2_font_size_last_edited=”off|desktop” locked=”off” global_colors_info=”{}”]<\/p>\n
[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ custom_padding_last_edited=”on|phone” _builder_version=”4.20.2″ _module_preset=”default” background_color=”#FFFFFF” custom_margin=”||||false|false” custom_padding=”||||false|false” custom_padding_tablet=”||||false|false” custom_padding_phone=”0px||0px||false|false” global_colors_info=”{}”][et_pb_row column_structure=”1_2,1_2″ make_equal=”on” _builder_version=”4.20.2″ _module_preset=”default” width_tablet=”” width_phone=”90%” width_last_edited=”on|phone” custom_margin=”||0px||false|false” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.19.5″ _module_preset=”default” global_colors_info=”{}”][et_pb_text admin_label=”PHIP Gene” _builder_version=”4.21.0″ text_font=”Montserrat|500||on|||||” text_text_color=”#353740″ text_font_size=”16px” text_letter_spacing=”3px” custom_margin=”||20px||false|false” custom_padding=”||||false|false” animation_direction=”bottom” locked=”off” global_colors_info=”{}”]PHIP<\/em>-Gene (6q14.1)[\/et_pb_text][et_pb_divider color=”#E02B20″ divider_weight=”3px” _builder_version=”4.20.2″ _module_preset=”default” max_width=”60px” custom_margin=”||15px||false|false” global_colors_info=”{}”][\/et_pb_divider][et_pb_image src=”https:\/\/chungjansensyndrome.eu\/wp-content\/uploads\/2023\/04\/in-short-mobile.jpeg” title_text=”in-short-mobile” disabled_on=”off|on|on” _builder_version=”4.20.2″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.19.5″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ make_equal=”on” _builder_version=”4.20.2″ _module_preset=”default” width_tablet=”” width_phone=”90%” width_last_edited=”on|phone” custom_margin=”0px||||false|false” custom_padding=”0px||||false|false” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.19.5″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.21.0″ text_font=”Montserrat||||” text_text_color=”#747d88″ text_line_height=”1.8em” link_font=”|700|||||||” link_text_color=”#0d4b7e” header_font=”||||||||” header_3_font_size=”18px” text_orientation=”justified” custom_margin=”||||false|false” custom_padding=”||||false|false” animation_direction=”top” text_font_size_tablet=”” text_font_size_phone=”16px” text_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n Chung-Jansen syndrome is a rare disorder- also called PHIP<\/em>-related disorder. The syndrome is caused by a heterozygous mutation along the PHIP<\/em> gene. Individuals with this disorder typically have developmental delay, behavioral problems, and are at risk for obesity. At present, the syndrome has been diagnosed in about 900 people worldwide. This number, however, is growing rapidly.<\/p>\n Young children often have feeding difficulties and delayed developmental milestones like rolling, crawling, standing straight and walking. Delayed motor development is partly related to the low muscle tone (hypotonia). Many children and adults with the disorder complain of fatigue and may need to use aids such as a wheelchair. Speech and fine motor skills are often delayed as well.<\/p>\n [\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.19.5″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.21.0″ text_font=”Montserrat||||” text_text_color=”#747d88″ text_line_height=”1.8em” link_font=”|700|||||||” link_text_color=”#0d4b7e” header_font=”||||||||” header_3_font_size=”18px” text_orientation=”justified” custom_margin=”||||false|false” custom_padding=”||||false|false” animation_direction=”top” text_font_size_tablet=”” text_font_size_phone=”16px” text_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n