Rx ENT, Oral and Dental Health (A – Z)
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Amelogenesis Imperfecta Caused by FAM20A Mutation
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Amelogenesis imperfecta (AI) is a group of genetic conditions where the hard outer layer of the teeth, called enamel, does not form in the normal way. When AI ...

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Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome (AIGFS)
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Amelogenesis imperfecta and gingival fibromatosis syndrome is a rare, inherited condition that mainly affects the mouth and teeth. People are born with a ...

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Oral and Dental Diseases
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Oral and dental diseases includeĀ tooth decay (cavities), gum disease (periodontal disease), tooth loss, and oral cancer, which are largely preventable through ...

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Enamel-Renal-Gingival Syndrome
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Enamel-Renal-Gingival Syndrome is a rare inherited condition that mainly affects the teeth, gums, and kidneys. Children are usually born healthy, but the ...

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Amelogenesis Imperfecta Type 1G
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Amelogenesis imperfecta type 1G is a rare, inherited condition where the outer hard covering of the teeth (the enamel) does not form normally. In this type, ...

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X-linked Amelogenesis Imperfecta 1 (AMELX-related AI)
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X-linked amelogenesis imperfecta 1 is a genetic condition that affects how tooth enamel forms. ā€œX-linkedā€ means the change is on the X chromosome. The main ...

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AMELX Amelogenesis Imperfecta
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AMELX amelogenesis imperfecta is a hereditary (genetic) enamel problem caused by a change (mutation) in a gene called AMELX on the X-chromosome. The AMELX gene ...

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Snow-Capped Teeth
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Snow-capped teeth describes a special look of tooth enamel where the biting edges of front teeth or the chewing tips of back teeth appear bright white and ...

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Amelogenesis Imperfecta, Hypomaturation Type (Snow-Capped Teeth Variant)
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Amelogenesis imperfecta (AI) is a group of rare, inherited conditions that affect the outer layer of the teeth, called enamel. In AI, enamel does not form or ...

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Amelogenesis Imperfecta (AI) Caused by Mutation in the AMELX Gene
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Amelogenesis imperfecta (AI) is a group of genetic conditions that affect the hard outer cover of the teeth, called enamel. People with AI are born with enamel ...

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Amelogenesis Imperfecta Type 1E (AI1E)
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Amelogenesis imperfecta type 1E is a rare, inherited enamel disorder. It belongs to the hypoplastic group of amelogenesis imperfecta (AI), which means the ...

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Hypoplastic Amelogenesis Imperfecta
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Hypoplastic amelogenesis imperfecta is a genetic problem of tooth enamel formation. ā€œHypoplasticā€ means there is too little enamel. The enamel that forms is ...

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Amelogenesis Imperfecta (AI) Type 1
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Amelogenesis imperfecta (AI) type 1 is the hypoplastic type of AI. That means the enamel is too thin or only partly formed from birth. Enamel is the hard, ...

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Bilingual Aphasia
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Bilingual aphasia is a language problem that happens after brain injury in a person who uses two languages.Aphasia means trouble using or understanding ...

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Nasal Dysbiosis
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Nasal dysbiosis happens when the tiny living creatures (microbes) that normally keep your nose healthy get out of balance. In very simple terms, your nose has ...

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Trochlear Nerve Palsy
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Trochlear nerve palsy is a disorder affecting the fourth cranial nerve (trochlear nerve), which controls the superior oblique muscle of the eye. When this ...

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Congenital Ophthalmoparesis
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Congenital ophthalmoparesis is a rare condition present from birth in which one or more of the extraocular muscles fail to function normally, leading to ...

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Flaccid Dysarthria
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Flaccid dysarthria is a motor speech disorder that arises when the lower motor neurons (LMNs) or peripheral nerves supplying the muscles of speech are damaged. ...

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Dysarthria
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Dysarthria is a motor speech disorder characterized by weakened, slow, or uncoordinated movements of the muscles used for speaking. Unlike aphasia, which ...

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Visual Object Agnosia
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Visual Object Agnosia is a neurological disorder characterized by the inability to recognize, identify, or interpret visually presented objects, despite intact ...

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