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  2. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Distal 18q- is a rare disorder caused by a deletion of genetic material in the distal section of the long arm of chromosome 18. It affects various systems and causes intellectual disability, congenital anomalies, dysmorphic features, and increased risk of infections and psychiatric conditions.

  3. Ring chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_18

    The ring is formed when the caps on both the long arm (q) and the short arm (p) of one copy of chromosome 18 are lost and the new ends re-join to form the ring. Because the ring involves deletions of both the long arm (18q-) and the short arm (18p-) of chromosome 18, individuals with ring 18 can have features of both 18p-as well as distal 18q-.

  4. Pierre Robin sequence - Wikipedia

    en.wikipedia.org/wiki/Pierre_Robin_sequence

    Pierre Robin sequence is a congenital defect that causes facial abnormalities, such as micrognathia, glossoptosis, and cleft palate. It may be due to mechanical or genetic factors, and can be associated with other disorders or syndromes.

  5. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    Learn about chromosome 18, one of the 23 pairs of chromosomes in humans. Find out its length, number of genes, partial gene list, and diseases related to its abnormalities.

  6. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere ) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [ 1 ]

  7. Beckwith–Wiedemann syndrome - Wikipedia

    en.wikipedia.org/wiki/Beckwith–Wiedemann_syndrome

    Beckwith–Wiedemann syndrome (/ ˈ b ɛ k ˌ w ɪ θ ˈ v iː d ə. m ə n /; abbreviated BWS) is an overgrowth disorder usually present at birth, characterized by an increased risk of childhood cancer and certain congenital features.

  8. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    Individuals with PKS present prenatally or at birth with multiple birth defects.These defects include: brain atrophy, agenesis of the corpus callosum, polymicrogyria of the brain, and/or spot calcifications in the brain's lateral sulcus; deafness and/or blindness; autonomic nervous system dysfunctions such as anhidrosis, hypohidrosis, and/or episodic spells of hyperventilation interspersed ...

  9. Tricho–dento–osseous syndrome - Wikipedia

    en.wikipedia.org/wiki/Tricho–dento–osseous...

    Esthetic procedures such as dental crown (dentistry) or veneer (dentistry) are often performed to improve the physical look of the teeth and to strengthen the weak enamel caused by TDO. [ 1 ] Root canal procedure: unhealthy or injured tooth, subsequent creation of an access cavity with a dental handpiece, cleaning & shaping the root canals with ...