Cutis laxa in Child
The AR forms are typically evident at birth and may be accompanied by early-onset emphysema:
- AR form, type 1 (1A-fibulin 5, 1B-fibulin 4, 1C-latent transforming growth factor [TGF] beta binding protein-4 gene mutations) – Characteristic skin findings beginning at birth. Systemic involvement is more severe, resulting in high mortality in early childhood.
- AR form, type 2 – Type 2A (wrinkled skin syndrome) is associated with defective N- and O-glycosylation. There is a strong female predominance. It is associated with severe neurological manifestations including pachygyria, microcephaly, seizures, and Dandy-Walker malformation. Type 2B presents with wrinkled inelastic skin, notably on the dorsal acral surfaces and abdomen, along with musculoskeletal and neurological abnormalities. Patients display facial dysmorphism, with triangular facies and progeroid appearance.
- AR, type 3 (De Barsy syndrome / progeroid syndrome of De Barsy / cutis laxa-corneal clouding-intellectual disability syndrome) – Associated with bilateral corneal opacification, progeroid appearance, decreased subcutaneous fat, and athetoid movements beginning early in life.
The AD form, the mildest with the fewest internal manifestations, is more likely to develop in later life, and patients have a normal lifespan.
Inherited syndromes with cutis laxa include:
- Macrocephaly, alopecia, cutis laxa, and scoliosis (MACS) syndrome – Notable for macrocephaly, facial dysmorphism, gingival hypertrophy, dental abnormalities, sparse hair, high-pitched voice, and musculoskeletal abnormalities. Ocular, neurologic, and respiratory symptoms are absent.
- Arterial tortuosity syndrome – AR disorder due to SLC2A10 mutation. There is variable skin laxity, cleft palate, hypertelorism, bifid uvula. Arterial anomalies result in early death.
- Medication-induced cutis laxa causes acquired Type 1 cutis laxa, sometimes with generalized elastolysis. Reported onset is within weeks to months of starting the medication. It has been associated with the use of penicillin and isoniazid. Neonatal cutis laxa can occur in newborns of mothers treated with penicillamine (or, less frequently, penicillin or isoniazid).
- Cutis laxa may be associated with urticaria or angioedema, malignancies (eg, multiple myeloma, lymphoma), congenital hemolytic anemia, an arthropod bite reaction, extensive inflammatory skin disease (eg, atopic dermatitis, erythema multiforme, dermatitis herpetiformis, sarcoidosis, Sweet syndrome, interstitial granulomatous dermatitis), infections (eg, Toxocara canis, Borrelia burgdorferi, Treponema pallidum, Onchocerca volvulus), connective tissue diseases (eg, rheumatoid arthritis, systemic lupus erythematosus, lupus panniculitis), celiac disease, nephritic syndrome, alpha-1-antitrypsin deficiency, mastocytosis, and amyloidosis.
- Marshall syndrome – A form of acquired cutis laxa seen primarily in infants and young children following the onset of Sweet syndrome-like neutrophilic dermatosis.
For more information on the AD form, see OMIM.
Q82.8 – Other specified congenital malformations of skin
58588007 – Cutis laxa
- Actinic elastosis
- Corticosteroid-induced atrophy
- Mid-dermal elastolysis
- Pseudoxanthoma elasticum
- Marfan syndrome
- Ehlers-Danlos syndrome
- Tenascin-X deficiency
- Costello syndrome
- SCARF syndrome
- Larsen-like syndrome
- Donohue syndrome
- Finnish-type amyloidosis
- Cranioectodermal dysplasia (Sensenbrenner syndrome)
- Circumferential skin creases, Kunze type
- "Michelin tire baby" syndrome