Dyskeratosis congenita (DKC) is a rare progressive bone marrow failure syndrome characterized by cutaneous pigmentation, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, ...
Dyskeratosis congenita (Zinsser-Cole-Engman syndrome) Dyskeratosis congenita, like Werner syndrome, results in premature aging and is considered a progeroid disease.
Dyskeratosis congenita is a congenital disease, meaning it is present at birth. It was initially thought to only affect the skin and nails, but today experts understand that dyskeratosis congenita in its most severe form causes bone marrow failure.
Fanconi anemia Dyskeratosis congenita Shwachman-Diamond syndrome Amegakaryocytic thrombocytopenia Myelodysplastic syndrome ...
X-Linked Dyskeratosis Congenita X-Linked Dyskeratosis Congenitas X-Linked Hypophosphatemic Rickets X-Linked Ichthyoses X-Linked Ichthyosis X-Linked Lymphoproliferative Disorder X-Linked Lymphoproliferative Disorders ...
Dyskeratosis Congenita Dyskeratosis Congenita Syndrome Dyskeratosis Follicularis Dyslexia Dyslexia Dyslexia / Learning Disabilities Helpline - Support Group Dyslexia Support 2 - Support Group ...
elegans genome, DSORD, CSB (ORA), delta Bilirubin, Determinism, Genetic, Dyskeratosis Congenita, X Linked, Dysmotility, Esophageal, Epiretinal Membranes, Factor, Political, Feline Leukemia Viruses, gamma Interferon, Recombinant, Gross Virus, ...
Neutropenia can also result from bone marrow failure due to rare syndromes (eg, cartilage-hair hypoplasia, Chédiak-Higashi syndrome, dyskeratosis congenita, glycogen storage disease type IB, Shwachman-Diamond syndrome).
hair loss Dubowitz Syndrome ... sparse scalp hair Dyskeratosis Congenita ... sparse hair Dyskeratosis congenita of Zinsser-Cole-Engman ... sparse hair Dystrophic epidermolysis bullosa ... sparse hair ...
Oral squamous cell carcinoma may develop in patients with Fanconi anemia, dyskeratosis congenita (a rare bone marrow failure syndrome), chronic graft-versus-host disease, epidermolysis bullosa, xeroderma pigmentosum, ...
Some inherited genetic disorders can lead to aplastic anemia. These include Fanconi anemia, Shwachman-Diamond syndrome, and dyskeratosis congenita. Diagnosis ...
Dyskeratosis Congenita Dyslexia Dysphasia see Aphasia Dyspraxia Dystonia Dystrophia Myotonica see Myotonic Dystrophy/Congenital Myotonic Dystrophy Dystrophic Epidermolysis Bullosa see Epidermolysis Bullosa ...
Dynabac Dynacin Dynacirc Dynacirc cr Dynapen Dynein Dyrenium DYS Dysarthria Dyscalculia Dyscrasia Dysentery Dysentery, amebic Dysfunction Dysfunction, erectile Dysfunctional Dysgenesis Dysgeusia Dysgraphia Dyshidrotic eczema Dyskeratosis congenita ...
See also: Keratosis, Cancer, Anemia, Deficiency, Symptom
 
|