Ad
related to: congenital syndromes list of medications for adults- Find a Doctor
Meet with our experts to diagnose
your symptoms and receive treatment
- ACHD in Pregnancy
One of the nations largest programs
Women with congenital heart defects
- Prepare For Your Visit
What to bring to your visit
plus heart & vascular resources
- Patient Testimonials
Hear from our patients
about their Ohio State experience
- Multidisciplinary Care
Care from birth to adulthood
with a trusted care team
- Should I See A Heart Doc
Talk to your doc about your heart
and learn what to ask
- Find a Doctor
Search results
Results From The WOW.Com Content Network
Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome; Congenital diaphragmatic hernia (CDH) Congenital Disorder of Glycosylation (CDG) Congenital hyperinsulinism; Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins; Costello syndrome; Craniopagus ...
Lesch–Nyhan syndrome; Lethal congenital contracture syndrome; Lethal white syndrome; Leukotriene receptor antagonist-associated Churg–Strauss syndrome; Levator ani syndrome; Leydig cell hypoplasia; Liddle's syndrome; Liebenberg syndrome; LIG4 syndrome; Lima syndrome; Limb girdle syndrome; Limber tail syndrome; Limb–mammary syndrome ...
Disability-adjusted life year for childhood-cluster diseases per 100,000 inhabitants. These include pertussis , poliomyelitis , diphtheria , measles , and tetanus . no data
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.
LAMA2-related (merosin deficient) congenital muscular dystrophy (Emery–Dreifuss muscular dystrophy) Collagen VI-related muscular dystrophy (Bethlem myopathy, Ullrich congenital muscular dystrophy) α-Dystroglycanopathies (Walker–Warburg syndrome, muscle-eye-brain disease) Laminopathies
The drug was approved as an add-on treatment to diet to reduce triglycerides in adults with the condition. The disorder affects fewer than 5,000 people in the U.S., according to government data ...
A congenital malformation is a physical anomaly that is deleterious, i.e. a structural defect perceived as a problem. A typical combination of malformations affecting more than one body part is referred to as a malformation syndrome. [citation needed] Some conditions are due to abnormal tissue development: