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  2. Beckwith–Wiedemann syndrome - Wikipedia

    en.wikipedia.org/wiki/BeckwithWiedemann_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. A minority (<15%) of cases of BWS are familial, meaning that a close relative may also have BWS, and parents ...

  3. Diffuse capillary malformation with overgrowth - Wikipedia

    en.wikipedia.org/wiki/Diffuse_capillary...

    Presence of neurological abnormality or macrocephaly can suggest macrocephaly-capillary malformation syndrome. Hemihypertrophy-multiple lipomatosis or Beckwith–Wiedemann syndrome are diseases with total hypertrophy and are associated with an increased risk of Wilms' tumor. [26] [27] About 10% of DCMO cases present with total hemihypertrophy. [3]

  4. Omphalocele - Wikipedia

    en.wikipedia.org/wiki/Omphalocele

    Omphalocele occurs in 1 in 4,000 births and is associated with a high rate of mortality (25%) and severe malformations, such as cardiac anomalies (50%), neural tube defect (40%), exstrophy of the bladder and Beckwith–Wiedemann syndrome. Approximately 15% of live-born infants with omphalocele have chromosomal abnormalities.

  5. J. Bruce Beckwith - Wikipedia

    en.wikipedia.org/wiki/J._Bruce_Beckwith

    John Bruce Beckwith (September 18, 1933 – January 21, 2025) was an American pediatric pathologist known for helping to identify Beckwith-Wiedemann syndrome, which is partly named after him. He is also known for his role as reference pathologist for the National Wilms Tumor Study Group , a position he held from 1969 until his retirement thirty ...

  6. H19 (gene) - Wikipedia

    en.wikipedia.org/wiki/H19_(gene)

    283120 n/a Ensembl ENSG00000130600 ENSG00000288237 n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) Chr 11: 2 – 2 Mb n/a PubMed search n/a Wikidata View/Edit Human H19 is a gene for a long noncoding RNA, found in humans and elsewhere. H19 has a role in the negative regulation (or limiting) of body weight and cell proliferation. This gene also has a role in ...

  7. List of congenital disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_congenital_disorders

    Cat eye syndrome; Caudal regression syndrome; Sotos syndrome Cerebral Gigantism; CHARGE syndrome; Chromosome 16 abnormalities; Chromosome 18 abnormalities; Chromosome 20 abnormalities; Chromosome 22 abnormalities; Cleft lip/palate; Cleidocranial dysostosis; Club foot; Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome

  8. All About the First Actor with Down Syndrome to Lead an ...

    www.aol.com/first-actor-down-syndrome-lead...

    The 37-year-old is the first actor with Down syndrome to ever lead an action movie, in the upcoming film Strait Undercover, produced by Fish & Crown Creative, according to the Today show.

  9. Large for gestational age - Wikipedia

    en.wikipedia.org/wiki/Large_for_gestational_age

    Genetic disorders of overgrowth (e.g. Beckwith–Wiedemann syndrome, Sotos syndrome, Perlman syndrome, Simpson-Golabi-Behmel syndrome) are often characterized by macrosomia. [ 25 ] [ 26 ] Other risk factors