estriol has been researched along with De Lange Syndrome in 2 studies
hormonin: estrogen replacement; each tablet contains 600 ug micronized 17beta-estradiol, 270 ug estriol and 1.4 mg estrone
chlorapatite : A phosphate mineral with the formula Ca5(PO4)3Cl.
De Lange Syndrome: A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231)
Excerpt | Relevance | Reference |
---|---|---|
"The prenatal diagnosis of diaphragmatic hernia with associated anomalies should prompt consideration of an underlying genetic etiology." | 1.31 | Fetal diaphragmatic hernia and upper limb anomalies suggest Brachmann-de Lange syndrome. ( Bianchi, DW; Craigo, SD; Marino, T; Simpson, LL; Wheeler, PG, 2002) |
"The significance of association between Cornelia de Lange syndrome and compromised synthesis of PAPP-A is discussed." | 1.27 | Pregnancy-associated plasma protein A: a possible marker in the classification and prenatal diagnosis of Cornelia de Lange syndrome. ( Beck, B; Chemnitz, J; Grudzinskas, JG; Ipsen, L; Poulsen, HK; Teisner, B; Westergaard, JG, 1983) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Westergaard, JG | 1 |
Chemnitz, J | 1 |
Teisner, B | 1 |
Poulsen, HK | 1 |
Ipsen, L | 1 |
Beck, B | 1 |
Grudzinskas, JG | 1 |
Marino, T | 1 |
Wheeler, PG | 1 |
Simpson, LL | 1 |
Craigo, SD | 1 |
Bianchi, DW | 1 |
2 other studies available for estriol and De Lange Syndrome
Article | Year |
---|---|
Pregnancy-associated plasma protein A: a possible marker in the classification and prenatal diagnosis of Cornelia de Lange syndrome.
Topics: Adult; De Lange Syndrome; Estriol; Female; Histocytochemistry; Humans; Infant, Newborn; Placenta; Pl | 1983 |
Fetal diaphragmatic hernia and upper limb anomalies suggest Brachmann-de Lange syndrome.
Topics: Adult; alpha-Fetoproteins; Chorionic Gonadotropin; De Lange Syndrome; Estriol; Fatal Outcome; Female | 2002 |