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Medical condition
Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is
Poikiloderma
Medical condition
Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened
Poikiloderma vasculare atrophicans
Poikiloderma_vasculare_atrophicans
Rare autosomal recessive skin condition
has been implicated in the syndrome. Sun-sensitive rash with prominent poikiloderma and telangiectasias Juvenile cataracts Saddle nose Congenital bone defects
Rothmund–Thomson_syndrome
Medical condition
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a type of epidermolysis bullosa, a rare congenital disease
Kindler_syndrome
Breast cleavage
right third intercostal nerve through its anterior cutaneous branch. Poikiloderma of Civatte, a condition of dilated blood vessels and red to red-brown
Intermammary_cleft
Medical condition
Poikiloderma of Civatte is a cutaneous condition and refers to reticulated red to red-brown skin patches with telangiectasias. It is identifiable as a
Poikiloderma_of_Civatte
Autoimmune diseases of the skin
Side effects may be mild, such as itchiness, folliculitis, sunburn, poikiloderma, and a theoretical risk of nonmelanoma cancer or melanoma has been suggested
Psoriasis
Condition characterized by absence of pigment
perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis Linear Incontinentia
Albinism_in_humans
Rare X-linked dominant genetic disorder
Incontinentia pigmenti (IP) is a rare X-linked dominant genetic disorder that affects the skin, hair, teeth, nails and central nervous system. It is named
Incontinentia_pigmenti
poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with
List_of_skin_conditions
Any medical condition that affects the integumentary system
hours) Granuloma Livedo Purpura Erythema (redness) Horn (a cell type) Poikiloderma Hyperkeratosis Parakeratosis Hypergranulosis Acanthosis Papillomatosis
Skin_condition
Medical condition
phototoxicity, nevus of Ota, café au lait macules, seborrheic keratosis, Poikiloderma of Civatte, acquired bilateral nevus of ota-like macules (Hori's nevus)
Melasma
Medical condition
Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood
Hereditary sclerosing poikiloderma
Hereditary_sclerosing_poikiloderma
Medical condition
fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis is a rare genetic syndrome characterised by poikiloderma, tendon contractures
Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis
Hereditary_fibrosing_poikiloderma_with_tendon_contractures,_myopathy,_and_pulmonary_fibrosis
Skin treatment with flashlamps
including photodamage induced dyspigmentation and vascular changes, poikiloderma of Civatte, rosacea, acne vulgaris, sebaceous gland hyperplasia, broken
Intense_pulsed_light
retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary acrokeratotic Weary type Poikiloderma of Kindler Poikiloderma of Rothmund–Thomson
List_of_diseases_(P)
Medical condition
Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, is a rare autosomal dominant form of
Naegeli–Franceschetti–Jadassohn syndrome
Naegeli–Franceschetti–Jadassohn_syndrome
Condition in which the jaw is small
scapular anomalies Pierre Robin syndrome-faciodigital anomaly syndrome Poikiloderma with neutropenia Polymicrogyria with or without vascular-type Ehlers–Danlos
Micrognathism
Topics referred to by the same term
alignment, a thin-film-transistor liquid-crystal display technology Poikiloderma vasculare atrophicans, a skin disease Polyvinyl acetate, an adhesive
PVA
Group of genetic disorders affecting motor neurons controlling the lower limbs
Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive
Hereditary_spastic_paraplegia
Medical condition
Acquired perforating dermatosis Skin ulcer Pyoderma gangrenosum Other Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum/Pseudo-ainhum
Burn_scar_contracture
Medical condition
Ectodermal dysplasias Clouston's hidrotic ectodermal dysplasia Acrokeratotic poikiloderma Dermatopathic pigmentosa reticularis Syndromic keratodermas Vohwinkel
Keratoderma
Class of enzymes that unpack genetic material
syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts
Helicase
Medical condition
lichenoides et varioliformis acuta Lymphomatoid papulosis Mycosis Fungoides Poikiloderma vasculare atrophicans List of cutaneous conditions Sehgal VN, Srivastava
Parapsoriasis
Medical condition
the hands and feet, and typical facial changes. Hereditary sclerosing poikiloderma Skin lesion "Mandibuloacral dysplasia". Genetic and Rare Diseases. NIH
Mandibuloacral_dysplasia
Medical condition
characteristics sometimes associated with this disorder are growth retardation and poikiloderma. Although the presentation of BGS may differ between individuals, these
Baller–Gerold_syndrome
Protein-coding gene in the species Homo sapiens
Gannavarapu A, Clericuzio CL, et al. (2004). "Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients". Am. J. Med. Genet
RECQL4
Medical conditions
coeliac disease. Rothmund–Thomson syndrome. Rothmund–Thomson syndrome, or poikiloderma congenitale, is a rare disorder, generally attributed to mutations of
Gluten-sensitive enteropathy–associated conditions
Gluten-sensitive_enteropathy–associated_conditions
Medical condition
which occur in >75% of patients, include erythroderma, pruritus, eczema, poikiloderma, urticarial, and episodic angioedema. The symptom of episodic angioedema
Lymphocyte-variant hypereosinophilia
Lymphocyte-variant_hypereosinophilia
Spastic paraplegia nephritis deafness Spastic paraplegia neuropathy poikiloderma Spastic paraplegia type 1, X-linked Spastic paraplegia type 2, X-linked
List_of_diseases_(S)
pseudoobstruction patent ductus Nathalie syndrome Native American myopathy Navajo poikiloderma Naxos disease Necrotizing arteriolitis Necrotizing encephalopathy, infantile
List_of_diseases_(N)
Medical condition
characterized by deep furrowing of the skin. List of cutaneous conditions Poikiloderma of Civatte Solar elastosis Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo
Cutis_rhomboidalis_nuchae
Medical condition
Baller–Gerold syndrome (BGS) Short broad head, bulging eyes, flat forehead, poikiloderma, radial deformity with reduced number of digits, underdeveloped or missing
Saethre–Chotzen_syndrome
Medical condition
inherited in an autosomal dominant manner. List of cutaneous conditions Poikiloderma vasculare atrophicans "OMIM Entry - 130100 - ELASTOSIS PERFORANS SERPIGINOSA;
Elastosis perforans serpiginosa
Elastosis_perforans_serpiginosa
Medical condition
a common associate of retiform parapsoriasis, can be accompanied by poikiloderma vasculare atrophicans, and can in rare occasions be a precursor to cutaneous
Large_plaque_parapsoriasis
Medical condition
tissue, usually occurs within the area of these plaques. Parapsoriasis Poikiloderma vasculare atrophicans List of cutaneous conditions Lambert WC, Everett
Retiform_parapsoriasis
blastoma; 601200; DICER1 Pneumothorax, primary spontaneous; 173600; FLCN Poikiloderma with neutropenia; 604173; C16orf57 Polycystic kidney and hepatic disease;
List_of_OMIM_disorder_codes
Medical condition
characterized by a prominent palmoplantar keratoderma. Hereditary sclerosing poikiloderma List of cutaneous conditions Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo
Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar_keratoderma–periodontitis_syndrome
POIKILODERMA
POIKILODERMA
POIKILODERMA
POIKILODERMA
Girl/Female
Finnish Latin
Rose.
Surname or Lastname
English
English : variant of Spragg.
Boy/Male
Arabic, Muslim
Contented; Satisfied
Girl/Female
Tamil
Surname or Lastname
English
English : habitational name for someone from Romford in Essex, probably so named from Old English rūm ‘broad’, ‘spacious’ + ford ‘ford’.
Boy/Male
Hindu, Indian, Kannada, Malayalam, Marathi, Sindhi, Telugu
Lord Krishna
Girl/Female
Tamil
Girl/Female
Tamil
Created
Girl/Female
Hindu
Name of An ancient king, Tested one or proven (son of Abhimanyu)
Boy/Male
Arabic, Parsi
Respected; Target; Aim
POIKILODERMA
POIKILODERMA
POIKILODERMA
POIKILODERMA
POIKILODERMA