Familial progressive hyperpigmentation is characterized by patches of hyperpigmentation, present at birth, which increase in size and number with age...
2 KB (120 words) - 00:38, 6 May 2024
syndrome (Griscelli syndrome type 1) Eruptive hypomelanosis Familial progressive hyperpigmentation Galli–Galli disease Griscelli syndrome type 2 (partial albinism...
198 KB (17,982 words) - 07:12, 15 July 2025
Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister–Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis...
42 KB (4,186 words) - 15:30, 17 July 2025
Prognathism dominant Progressive acromelanosis Progressive black carbon hyperpigmentation of infancy Progressive diaphyseal dysplasia Progressive external ophthalmoplegia...
24 KB (1,908 words) - 18:00, 4 March 2025
linked, recessive Exudative retinopathy, familial Extrapyramidal disorder Extrasystoles short stature hyperpigmentation microcephaly Eye defects arachnodactyly...
12 KB (918 words) - 00:54, 17 August 2024
arch, alongside extra-macular white deposits and localized areas of hyperpigmentation in the retinal pigment epithelium. The heads of the optic nerve start...
9 KB (1,047 words) - 19:01, 27 April 2025
deposits of amyloid. Females usually only have linear streaks of hyperpigmentation. The syndrome can also be referred to by the acronym X-Linked-PDR...
10 KB (886 words) - 20:01, 2 January 2024
hypocupremia hypobetalipoproteinemia Mental retardation hypotonia skin hyperpigmentation Mental retardation macrocephaly coarse facies hypotonia Mental retardation...
28 KB (2,470 words) - 15:50, 17 May 2025
type LM “Acquired” progressive lymphatic anomaly Primary lymphedema Nonne-Milroy syndrome Venous malformations Common VM Familial VM cutaneo-mucosal Blue...
17 KB (1,795 words) - 15:40, 25 May 2025
Mycosis fungoides (redirect from Mycosis fungoides, familial)
body, including the face and head regions. The symptoms displayed are progressive, with early stages consisting of lesions presented as scaly patches....
36 KB (3,994 words) - 08:50, 12 July 2025
Iron overload (redirect from Familial hemochromatosis)
cirrhosis, hypogonadism, cardiomyopathy, diabetes, arthritis, or hyperpigmentation is uncommon in current patients. Because of the severe sequelae of...
47 KB (4,889 words) - 04:18, 15 July 2025
Pigmented Freckles Lentigo Melasma Nevus Melanoma Postinflammatory hyperpigmentation Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma...
31 KB (2,435 words) - 19:01, 28 April 2025
patches on the glans and foreskin. It also causes post-inflammatory hyperpigmentation and melanosis. Adhesions, partial or complete, sub coronal and trans...
52 KB (5,779 words) - 17:46, 16 July 2025
plaques. This rash, after regressing, is likely to leave an area of hyperpigmentation that slowly fades. That said, a variety of other lesions can also...
66 KB (7,563 words) - 19:45, 27 June 2025
anomalies, hearing loss, and hypogonadism; 612391; SLC29A3 Hyperpigmentation, familial progressive; 145250; KITLG Hyperprolinemia, type I; 239500; PRODH Hyperprolinemia...
234 KB (18,877 words) - 18:07, 24 March 2025
consequences. Elevated ACTH is accompanied by and contributes to marked hyperpigmentation even in the newborn period. An inadequate cortisol response to stress...
20 KB (2,375 words) - 23:02, 12 March 2025
symptoms include: Intense itching Swelling Inflammation Depigmentation Hyperpigmentation Rash Nodules under the skin Skin atrophy Hanging groin (folds of inelastic...
62 KB (6,745 words) - 04:28, 13 June 2025