Ceruloplasmin
List of MeSH codes (C10)
... melas syndrome MeSH C10.228.140.163.100.540 - menkes kinky hair syndrome MeSH C10.228.140.163.100.545 - merrf syndrome MeSH ... lesch-nyhan syndrome MeSH C10.574.500.540 - menkes kinky hair syndrome MeSH C10.574.500.545 - myotonia congenita MeSH C10.574. ... lesch-nyhan syndrome MeSH C10.597.606.643.455.687 - menkes kinky hair syndrome MeSH C10.597.606.643.455.750 - ... cri-du-chat syndrome MeSH C10.597.606.643.210 - de lange syndrome MeSH C10.597.606.643.220 - down syndrome MeSH C10.597.606.643 ...
List of MeSH codes (C18)
MELAS syndrome MeSH C18.452.100.100.540 - Menkes kinky hair syndrome MeSH C18.452.100.100.545 - MERRF syndrome MeSH C18.452. ... MELAS syndrome MeSH C18.452.648.151.450 - menkes kinky hair syndrome MeSH C18.452.648.151.505 - MERRF syndrome MeSH C18.452. ... Menkes kinky hair syndrome MeSH C18.452.648.618.711 - paralyses, familial periodic MeSH C18.452.648.618.711.550 - hypokalemic ... Li-Fraumeni syndrome MeSH C18.452.284.600 - Nijmegen breakage syndrome MeSH C18.452.284.760 - Rothmund-Thomson syndrome MeSH ...
List of MeSH codes (C17)
Menkes kinky hair syndrome MeSH C17.800.428.200 - callosities MeSH C17.800.428.260 - cholesteatoma MeSH C17.800.428.260.300 - ... Tietze syndrome MeSH C17.300.200.310 - Ehlers-Danlos syndrome MeSH C17.300.200.425 - keloid MeSH C17.300.200.425.125 - acne ... Felty's syndrome MeSH C17.300.775.099.683 - rheumatoid nodule MeSH C17.300.775.099.774 - Sjögren syndrome MeSH C17.300.775.099. ... Stevens-Johnson syndrome MeSH C17.800.229.413 - erythema nodosum MeSH C17.800.229.413.800 - Sweet's syndrome MeSH C17.800. ...
Sex linkage
... kinky hair syndrome) Ornithine carbamoyltransferase deficiency Wiskott-Aldrich syndrome Various failures in the SRY genes White ... phosphate dehydrogenase deficiency Haemophilia A and B Hunter syndrome Inherited nephrogenic diabetes insipidus Menkes disease ... Alport syndrome Coffin-Lowry syndrome (CLS) Fragile X syndrome Idiopathic hypoparathyroidism Incontinentia pigmenti Rett ... Aarskog-Scott syndrome Adrenoleukodystrophy (ALD) Bruton's agammaglobulinemia Color blindness Complete androgen insensitivity ...
Menkes disease
Hair appears strikingly peculiar: kinky, colorless or silvery, and brittle. There can be extensive neurodegeneration in the ... Occipital horn syndrome (sometimes called X-linked cutis laxa or Ehlers-Danlos type 9) is a mild form of Menkes syndrome that ... Menkes disease (MNK), also known as Menkes syndrome, is an X-linked recessive disorder caused by mutations in genes coding for ... Menkes Disease at eMedicine "Menkes syndrome: MedlinePlus Genetics". medlineplus.gov. Retrieved 2022-10-10. Online Mendelian ...
Trichorrhexis nodosa
... kinky hair syndrome, Netherton's syndrome, hypothyroidism, or trichothiodystrophy. Examination of the hair shafts with a ... In some cases, trichorrhexis nodosa may be caused by an underlying disorder such as argininosuccinic aciduria, Menkes' ... hair growth hair appears patchy hair breaks easily close to scalp hair may have thickenings or nodes in the shaft ends of hair ... The hair should not be ironed. Excessively harsh shampoo should be avoided. Hair conditioners should be used.[citation needed] ...
List of skin conditions
... lines Melanonychia Menkes kinky hair syndrome (kinky hair disease, Menkes disease) Monilethrix (beaded hair) Muehrcke's nails ( ... Turner syndrome Ulnar-mammary syndrome Van Der Woude syndrome Von Hippel-Lindau syndrome Watson syndrome Werner syndrome (adult ... Gold dermatitis Hair bleach-induced Hair dye-induced Hair lotion-induced Hair spray-induced Hair straightener-induced Hair ... Uncombable hair syndrome (cheveux incoiffable, pili trianguli et canaliculi, spun-glass hair) Wooly hair nevus (woolly hair ...
List of MeSH codes (C16)
... fragile X syndrome MeSH C16.320.322.500.625 - Lesch-Nyhan syndrome MeSH C16.320.322.500.687 - Menkes kinky hair syndrome MeSH ... fragile X syndrome MeSH C16.320.400.525.625 - Lesch-Nyhan syndrome MeSH C16.320.400.525.687 - Menkes kinky hair syndrome MeSH ... MELAS syndrome MeSH C16.320.565.150.540 - Menkes kinky hair syndrome MeSH C16.320.565.150.545 - MERRF syndrome MeSH C16.320. ... Lesch-Nyhan syndrome MeSH C16.320.400.520 - Menkes kinky hair syndrome MeSH C16.320.400.525 - mental retardation, x-linked MeSH ...
Copper in biology
The brittle, kinky hypopigmented hair of steely appearance is due to a deficiency in an unidentified cuproenzyme. Reduced lysyl ... "Metabolic and molecular bases of Menkes disease and occipital horn syndrome". Pediatric and Developmental Pathology. 1 (1): 85- ... Menkes disease, a genetic condition of copper deficiency, was first described by John Menkes in 1962. It is a rare X-linked ... Even with early diagnosis and treatment, Menkes disease is usually fatal.[citation needed] Ongoing research into Menkes disease ...