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Symptoms and Testing information for PAFAH1B1 Gene Lissencephaly Type 1 Genetic Test

Lissencephaly, also known as “smooth brain” syndrome, is a rare, gene-linked brain malformation characterized by the absence of normal convolutions (folds) in the cerebral cortex and an abnormally small head (microcephaly). One of the genes associated with this condition is PAFAH1B1, and its mutations can lead to Lissencephaly Type 1. DNA Labs UAE offers a

Symptoms and Testing information for RELN Gene Lissencephaly Type 2 Norman-Roberts Type Genetic Test

Lissencephaly, meaning “smooth brain,” is a rare, genetic brain malformation characterized by the absence of normal convolutions (folds) in the cerebral cortex and an unusually small head (microcephaly). Among the various types of lissencephaly, Type 2, also known as Norman-Roberts syndrome, is distinguished by its genetic cause: mutations in the RELN gene. This article delves

Symptoms and Testing information for CDKN1C Gene IMAGE Syndrome Genetic Test

In the realm of genetic testing and diagnosis, understanding the nuances of specific syndromes is crucial for effective treatment and management. One such condition that has garnered attention in the medical community is IMAGE Syndrome, a rare disorder associated with mutations in the CDKN1C gene. At DNA Labs UAE, we offer a comprehensive genetic test

Symptoms and Testing information for TTC7A Gene Intestinal Atresia Multiple Genetic Test

DNA Labs UAE is at the forefront of genetic testing, offering a wide array of services designed to provide critical insights into various genetic conditions. Among the many tests provided, the TTC7A Gene Intestinal Atresia Multiple Genetic Test stands out for its significance in diagnosing a rare but severe genetic disorder. This test is crucial

Symptoms and Testing information for RET Gene Hirschsprung Disease Genetic Test

Hirschsprung disease is a rare disorder that affects the large intestine (colon) and causes problems with passing stool. It is present at birth (congenital) as a result of missing nerve cells in the muscles of the baby’s colon. A leading cause of this condition is mutations in the RET gene, among others. Recognizing the symptoms

Symptoms and Testing information for ZIC2 Gene Holoprosencephaly Type 5 Genetic Test

Understanding the genetic underpinnings of various conditions is crucial in the realm of medical science. One such condition that has garnered attention for its complexity and the critical need for accurate diagnosis is Holoprosencephaly Type 5, associated with mutations in the ZIC2 gene. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive

Symptoms and Testing information for FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test

Hydranencephaly is a rare neurological condition characterized by the absence of cerebral hemispheres, which are replaced by sacs filled with cerebrospinal fluid. One specific form of this condition, known as Fowler type, has been linked to mutations in the FLVCR2 gene. DNA Labs UAE is at the forefront of diagnosing this genetic disorder through the

Symptoms and Testing information for AHCY Gene Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase Genetic Test

Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase (AHCY) is a rare genetic disorder affecting the body’s ability to process certain amino acids properly. This condition can lead to a range of symptoms and health issues, making it crucial for individuals to understand the potential signs and the importance of genetic testing. DNA Labs UAE offers a

Symptoms and Testing information for ADNP Gene Helsmoortel-van der Aa Syndrome Genetic Test

ADNP syndrome, also known as Helsmoortel-van der Aa syndrome, is a rare genetic condition that has garnered attention in the medical community for its complex presentation and the diverse range of symptoms it encompasses. This condition is caused by mutations in the ADNP gene, which plays a crucial role in the development of the brain

Symptoms and Testing information for KIF1BP Gene Hirschsprung Disease Genetic Test

Hirschsprung disease is a rare congenital condition that affects the large intestine (colon) and causes problems with passing stool. The condition is present at birth (congenital) as a result of missing nerve cells in the muscles of the baby’s colon. A significant advancement in understanding the genetic basis of Hirschsprung disease has been the identification