স্বাস্থ্য এবং অসুস্থতা - জেনেটিক ডিসঅর্ডার

a genetic disorder characterized by connective tissue abnormalities, leading to various physical manifestations including tall stature, long limbs, joint hypermobility, and cardiovascular issues

মারফান সিন্ড্রোম

a genetic disorder causing the growth of tumors on nerves throughout the body, with varying symptoms and severity

নিউরোফাইব্রোমাটোসি

genetic disorder with characteristic facial features, short stature, developmental delays, and heart defects caused by mutations affecting cell signaling proteins

নুনান সিন্ড্রোম

a genetic disorder with symptoms like insatiable appetite, obesity, intellectual disability, and developmental delays caused by gene deletion or loss of function on chromosome 15

প্রাডার-উইলি সিনড্রোম

a genetic disorder in girls causing developmental regression, communication impairments, and neurological issues due to MECP2 gene mutations

রেট সিন্ড্রোম

a rare genetic disorder characterized by the progressive deterioration of the nervous system, typically leading to early childhood death

টে স্যাক্স রোগ

a genetic blood disorder characterized by reduced production of hemoglobin, leading to anemia, and it can range from mild to severe

থেলাসেমিয়া

a neurological disorder characterized by repetitive, involuntary movements and vocalizations called tics

ট্যুরেট সিন্ড্রোম

a genetic condition characterized by a lack of pigmentation in the skin, hair, and eyes, resulting in a significant reduction or absence of melanin

অ্যালবিনিজম

a rare genetic disorder with developmental delays, intellectual disability, speech issues, and seizures, caused by gene mutations on chromosome 15

এঞ্জেলম্যান সিনড্রোম

a chronic inflammatory arthritis primarily affecting the spine, causing pain, stiffness, and potential fusion of the vertebrae

এনকাইলোজিং স্পন্ডিলাইটিস

a genetic disorder with craniofacial abnormalities, fused fingers or toes, and skeletal issues due to FGFR2 gene mutations

অপার্ট সিন্ড্রোম

a group of inherited neurological disorders affecting the peripheral nerves, leading to muscle weakness and atrophy, particularly in the feet and hands

চারকট-মেরি-টুথ রোগ

a genetic disorder causing hormonal imbalances and abnormal development of secondary sexual characteristics due to impaired cortisol production by the adrenal glands

জন্মগত অ্যাড্রেনাল হাইপারপ্লিশিয়া

a genetic disorder causing the production of thick and sticky mucus, affecting the respiratory and digestive systems and leading to various complications

সিস্টিক ফাইব্রোসিস

a genetic condition caused by the presence of an extra copy of chromosome 21, leading to intellectual disabilities, distinct facial features, and potential health issues

ডাউন সিনড্রোম

a group of connective tissue disorders causing joint hypermobility, skin that bruises easily, and other symptoms due to abnormal collagen production

এলার্স-ড্যানলস সিন্ড্রোম

a rare genetic disorder causing the build-up of a fatty substance in organs, leading to symptoms like pain, skin lesions, and organ damage

ফ্যাব্রি রোগ

a genetic disorder causing intellectual disability, developmental delays, and other symptoms due to a gene mutation that affects normal brain function

ভঙ্গুর X সিন্ড্রোম

a mostly inherited genetic disorder in which the blood does not clot properly, leading to excessive or spontaneous bleeding

হেমোফিলিয়া

a genetic disorder characterized by excessive absorption and accumulation of iron in the body, leading to potential organ damage

হেমো크োমেটোসিস

a genetic condition in males where there is an extra X chromosome, leading to developmental and hormonal differences

ক্লাইনفلটার সিন্ড্রোম

a genetic condition affecting females, where one of the X chromosomes is partially or completely missing, leading to various developmental and medical challenges

টার্নার সিন্ড্রোম

a bleeding disorder due to a deficiency or dysfunction of a blood clotting protein, leading to increased bleeding tendency

ভন উইলব্র্যান্ড রোগ

a rare genetic disorder characterized by distinctive facial features, developmental delays, and a unique cognitive profile, including strong verbal abilities and sociable personality traits

উইলিয়ামস সিন্ড্রোম

a hereditary neurodegenerative disorder characterized by progressive motor dysfunction, cognitive decline, and psychiatric symptoms

হান্টিংটনের রোগ

a genetic blood disorder where red blood cells assume an abnormal, crescent shape, leading to various complications

সিরপল সেল রোগ

a category of disorders characterized by the progressive degeneration or weakening of tissues, particularly muscles

ডিস্ট্রোফি