Title: Identify the types of transport

Natalie Rodríguez Collazo

Department of Nursing, NUC University

BIOL 1010 Introduction to Biology

Prof. Glenda L. August Robles

February 21, 2023

The syndrome that karyotype 1 shows us is Turner syndrome. This syndrome can be diagnosed by a test

with cells from the amniotic fluid while they are in the mother's belly. When they are newborns, the

diagnosis is detected when they begin to have heart problems or when they have some physical

characteristic. Certain girls may be diagnosed during adolescence since their growth rate is slow. The

genetic causes of this syndrome may be the lack of one copy of the X chromosome or there may be

changes in the said chromosome. The clinical picture for women with Turner syndrome is delayed

growth and shorter than normal height, among others. Life expectancy is shorter than that of other

people.
 The disease or syndrome that karyotype 2 shows us is Warkany syndrome. The diagnosis of this is

based on karyotype analysis or also on the detection of copy variation. The genetic cause of Warkany

syndrome is postzygotic separation, a mitotic error in the fetus. The clinical characteristic is facial

dysmorphia, deep palmar and plantar folds, and joint, cardiac, skeletal, and urinary anomalies. Some

patients with this syndrome have the absence of serious malformations, the life expectancy of these

people is normal.
 References:

Carbajal Cervantes, H. & Estrada Carbajal, A. c. (2017). Biology II: Series based on competencies and values.

National Human Genome Research Institute (NHGRI) (2011). Learning about Turner syndrome . Retrieved July 14, 2012.

Wisniewska M, Mazurek M. Trisomy 8 mosaicism syndrome. J Appl Genet. 2002.