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Hypotrichosis 1
- ... type Genetic Testing Registry: Wooly hair, autosomal recessive 1, with or without hypotrichosis Genetic Testing Registry: Hypotrichosis 6 Genetic Testing Registry: ...
- ... of the condition. Appelt-Gerken-Lenz syndrome Hypomelia hypotrichosis facial hemangioma syndrome Pseudothalidomide syndrome RBS Roberts-SC ... development, and human syndromes. Chromosoma. 2007 Feb;116(1):1-13. doi: 10.1007/s00412-006-0072- ...
- ... dwarfism) with other skeletal abnormalities; fine, sparse hair (hypotrichosis); and abnormal immune system function (immune deficiency) that ... Old Order Amish population, where it affects about 1 in 1,300 newborns. In people of Finnish ...
- ... hair syndrome Comel-Netherton syndrome Ichthyosiform erythroderma with hypotrichosis and hyper-IgE Ichthyosis linearis circumflexa ILC NETH ... LEKTI. G Ital Dermatol Venereol. 2013 Feb;148(1):37-51. Citation on PubMed Hovnanian A. Netherton ...
- ... People with monilethrix also have sparse hair growth (hypotrichosis) and short, brittle hair that breaks easily.Affected ... follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 2003 Apr 18; ...
- ... tend to have sparse scalp and body hair (hypotrichosis). The hair is often light-colored, brittle, and ... ectodermal dysplasia. It is estimated to occur in 1 in 20,000 newborns worldwide. Hypohidrotic ectodermal dysplasia ...
- ... features of oculodentodigital dysplasia include sparse hair growth (hypotrichosis); brittle nails; and a skin condition called palmoplantar ... unknown. It has been diagnosed in fewer than 1,000 people worldwide, although it is likely that ...
- ... tend to have sparse scalp and body hair (hypotrichosis). EDA-ID is also characterized by missing teeth ( ... type of EDA-ID is estimated to be 1 in 250,000 individuals. Only a few cases ...
- ... on their scalp where hair does not grow (hypotrichosis). About half of people with CIPA show signs ... 91. doi: 10.1016/s0959-4388(00)00092-1. Citation on PubMed Miranda C, Di Virgilio M, ...