User Posts: Dr. Harun Ar Rashid, MD - Arthritis, Bones, Joints Pain, Trauma, and Internal Medicine Specialist
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Vasterbotten Dystrophy
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Västerbotten dystrophy is a rare inherited eye disease that damages the retina and gradually reduces vision. It usually begins in childhood with night ...

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Bothnia Retinal Dystrophy (BRD)
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Bothnia retinal dystrophy (BRD) is a rare, inherited eye disease. It usually begins in childhood with night blindness and very slow dark adaptation. Over time, ...

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Bosley-Salih-Alorainy Syndrome (BSAS)
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Bosley–Salih–Alorainy syndrome (BSAS) is a very rare genetic condition caused by harmful changes (mutations) in a single gene called HOXA1. Children with BSAS ...

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Bosch-Boonstra-Schaaf Optic Atrophy–Intellectual Disability Syndrome (BBSOAS / NR2F1-Related Disorder)
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Bosch-Boonstra-Schaaf optic atrophy–intellectual disability syndrome (BBSOAS / NR2F1-related disorder) written in very simple English. BBSOAS is a rare, ...

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Bosch-Boonstra-Schaaf Optic Atrophy Syndrome
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Bosch-Boonstra-Schaaf optic atrophy syndrome is a rare, genetic neurodevelopmental condition. It is caused by a change (variant) in a gene called NR2F1. This ...

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BNAR Syndrome (Bifid Nose With or Without Anorectal and Renal Anomalies)
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BNAR Syndrome (Bifid Nose With or Without Anorectal and Renal Anomalies) is a very rare, inherited condition present at birth. The key feature is a split or ...

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Blue Rubber Bleb Nevus Syndrome (BRBNS)
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Blue rubber bleb nevus syndrome (BRBNS)—also called Bean syndrome—is a rare condition where a person has many abnormal venous malformations (enlarged, ...

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JavaScript Frameworks and Libraries List
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JavaScript frameworks and libraries are collections of pre-written JavaScript code designed to streamline and enhance web development. While both provide ...

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Beemer-Ertbruggen Syndrome
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Beemer-Ertbruggen syndrome is a lethal (life-limiting) pattern of birth differences first reported in two brothers from a consanguineous family. The children ...

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Exomphalos–Macroglossia–Gigantism Syndrome
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Exomphalos–Macroglossia–Gigantism Syndrome is an older name for Beckwith-Wiedemann syndrome (BWS). It is a congenital overgrowth condition. Babies are often ...

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Beckwith–Wiedemann Syndrome (BWS)
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Beckwith–Wiedemann syndrome (BWS) is a genetic growth disorder that starts before birth. Babies are often large, the tongue may be big, some organs are ...

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Pigmentary Hairy Epidermal Nevus
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Pigmentary hairy epidermal nevus is a birthmark or patch on the skin that looks darker than the surrounding skin and grows more hair than usual. Doctors use ...

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Becker Nevus Syndrome (BNS)
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Becker nevus syndrome (BNS) is a condition where a person has a Becker nevus on the skin and, on the same side of the body, also has under-development of ...

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Review Board Member
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Role and Responsibilities of a Review Board Member at RxHarun.com RxHarun.com is a trusted platform dedicated to delivering evidence-based, accessible, and ...

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Autoimmune, Genetics and Rare Diseases References
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   Disclaimer: Each person’s journey is unique, treatment plan, life style, food habit, hormonal condition, immune system, chronic disease ...

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Mixed Gallbladder Stones
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Mixed gallbladder stones are hard pebble-like lumps that form inside the gallbladder from more than one ingredient at the same time. Most stones are made ...

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Mixed Stones
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“Mixed stones” are solid lumps that form inside fluid-filled organs or ducts when different materials clump together. In everyday medicine, this term most ...

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Brown Pigment Stones
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Brown pigment stones are soft, brown-colored stones that form inside the bile ducts (the small tubes that carry bile from the liver to the intestine). Unlike ...

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Black Pigment Gallstones
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Black pigment gallstones are hard, dark stones that form inside your gallbladder. They are called “black” because they look jet-black or charcoal-black when ...

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Pigment gallstones
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Pigment gallstones are hard, pebble-like pieces that form inside the gallbladder or bile ducts. They are called “pigment” stones because they are made mainly ...

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