প্রবেশ করুন
স্বাস্থ্য এবং অসুস্থতা - জেনেটিক ডিসঅর্ডার
এখানে আপনি জেনেটিক ডিসঅর্ডার যেমন "অ্যালবিনিজম", "হিমোফিলিয়া", এবং "ডিস্ট্রোফি" সম্পর্কিত কিছু ইংরেজি শব্দ শিখবেন।
পর্যালোচনা
ফ্ল্যাশকার্ডসমূহ
বানান
কুইজ
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
নিউরোফাইব্রোমাটোসিস
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 - শ্যাস রোগ
a genetic blood disorder characterized by reduced production of hemoglobin, leading to anemia, and it can range from mild to severe
থ্যালাসেমিয়া
a neurological disorder characterized by repetitive, involuntary movements and vocalizations called tics
টুরেট 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
অ্যাঞ্জেলম্যান সিন্ড্রোম
a chronic inflammatory arthritis primarily affecting the spine, causing pain, stiffness, and potential fusion of the vertebrae
অ্যাঙ্কাইলোজিং স্পন্ডিলাইটিস
a genetic disorder with craniofacial abnormalities, fused fingers or toes, and skeletal issues due to FGFR2 gene mutations
অ্যাপার্ট সিন্ড্রোম
a group of inherited neurological disorders affecting the peripheral nerves, leading to muscle weakness and atrophy, particularly in the feet and hands
চারকোট-মেরি-দাঁতের রোগ
a genetic disorder causing hormonal imbalances and abnormal development of secondary sexual characteristics due to impaired cortisol production by the adrenal glands
জন্মগত অ্যাড্রিনাল হাইপারপ্লাসিয়া
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
Ehlers-Danlos 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 এক্স সিন্ড্রোম
a mostly inherited genetic disorder in which the blood does not clot properly, leading to excessive or spontaneous bleeding
হিমোফিলিয়া
a genetic disorder characterized by excessive absorption and accumulation of iron in the body, leading to potential organ damage
হেমোক্রোমাটোসিস
a genetic condition in males where there is an extra X chromosome, leading to developmental and hormonal differences
ক্লাইনফেল্টার 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 উইলেব্র্যান্ড 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
হান্টিংটন এর রোগ
a genetic blood disorder where red blood cells assume an abnormal, crescent shape, leading to various complications
সিকেল-সেল রোগ
