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| goltz [2026/08/02 15:44] – created Scott Larson | goltz [2026/08/02 15:57] (current) – Scott Larson | ||
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| ====== Goltz Syndrome ====== | ====== Goltz Syndrome ====== | ||
| - | + | ====Main Features==== | |
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| + | X-linked dominant multisystem ecto-mesodermal dysplasia affecting skin, skeleton, eyes, teeth, and face; ~90% of patients are female (M:F ~1:9), with hemizygous variants usually lethal in utero | ||
| + | * Blaschkolinear dermal hypoplasia (atrophic, erythematous, | ||
| + | * Soft yellow-pink nodular fat herniation into the dermis (60-70%) and telangiectasias (~80%) | ||
| + | * Blaschkolinear hyper- and hypopigmentation | ||
| + | * Periorificial and mucosal papillomas (perinasal, perioral, perianal, genital, laryngeal, esophageal) developing after infancy; may cause dysphagia or airway obstruction | ||
| + | * Ridged or dystrophic nails, micronychia; | ||
| + | * Limb malformations in >50%: ectrodactyly (" | ||
| + | * Osteopathia striata on long-bone metaphyseal radiographs: | ||
| + | * Proposed clinical criteria: at least 3 characteristic skin findings (patchy skin aplasia, nodular fat herniation, Blaschkolinear pigmentary change, telangiectasia, | ||
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| + | ====Eye Findings==== | ||
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| + | Ocular anomalies in ~15% (older series 20-40%), typically asymmetric, ranging from cosmetic to blinding | ||
| + | * Microphthalmia (most common) and anophthalmia | ||
| + | * Iris and chorioretinal coloboma; retinal and optic nerve dysplasia | ||
| + | * Lacrimal and nasolacrimal duct abnormalities | ||
| + | * Strabismus, cataract, corneal and anterior chamber defects | ||
| + | * Eyelid and conjunctival papillomas, ectropion, ptosis, sparse eyelashes and eyebrows | ||
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| + | ====Other Findings==== | ||
| + | * Craniofacial: | ||
| + | * Dental (20-50%): enamel hypoplasia, vertical grooving, hypodontia/ | ||
| + | * Ears and hearing: microtia, aural atresia, conductive and sensorineural hearing loss, vestibulocochlear dysplasia | ||
| + | * Central nervous system: intelligence usually normal, but intellectual disability, speech delay, microcephaly, | ||
| + | * Growth: short stature and growth failure; growth hormone deficiency investigated as a contributor | ||
| + | * Renal: fused or duplex kidney, renal hypoplasia, cysts | ||
| + | * Gastrointestinal and abdominal wall: omphalocele, | ||
| + | * Rare: giant cell tumor of bone, supernumerary nipple, athelia | ||
| + | * Histopathology: | ||
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| + | ====Etiology==== | ||
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| + | * X-linked dominant inheritance; | ||
| + | * Loss-of-function pathogenic variants in PORCN (Xp11.23), encoding porcupine O-acyltransferase, | ||
| + | * Male survivors result from postzygotic somatic mosaicism or 47,XXY (Klinefelter syndrome) | ||
| + | * Phenotypic variability reflects random X-inactivation (functional mosaicism) and postzygotic mosaicism; no genotype-phenotype correlation established | ||
| + | * Point and small mutations predominate in sporadic cases, larger deletions in familial cases; germline mosaicism reported | ||
| + | * Blood DNA testing may be negative in mosaic patients; testing DNA from affected skin or fibroblasts improves diagnostic yield | ||
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| + | ====References==== | ||
| + | * [[https:// | ||
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