Parry–Romberg syndrome

Short description: Very Rare disease involving degeneration of tissues beneath the skin

Parry–Romberg syndrome

Other names| Progressive hemifacial atrophy
a 17-year-old girl with Parry–Romberg syndrome. The subcutaneous tissue and underlying facial muscles on the right side of the face are severely atrophic, while the left side is unaffected.

Parry–Romberg syndrome (PRS) is a rare disease presenting in early childhood[1] characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body.[2] An autoimmune mechanism is suspected, and the syndrome may be a variant of localized scleroderma, but the precise cause and pathogenesis of this acquired disorder remains unknown. It has been reported in the literature as a possible consequence of sympathectomy. The syndrome has a higher prevalence in females and typically appears between 5 and 15 years of age. There has been only one case report of the syndrome appearing in older adults: a 43-year-old woman with symptoms appearing at the age of 33.[3]

In addition to the connective tissue disease, the condition is sometimes accompanied by neurological, ocular, and oral symptoms. The range and severity of associated symptoms and findings are highly variable.

## Contents

* 1 Signs and symptoms
* 1.1 Skin and connective tissues
* 1.2 Neurological
* 1.3 Ocular
* 1.4 Oral
* 2 Causes
* 3 Diagnosis
* 4 Management
* 4.1 Medical
* 4.2 Surgical
* 5 Epidemiology
* 6 History
* 7 See also
* 8 References
* 9 Further reading
* 10 External links

## Signs and symptoms

### Skin and connective tissues

An axial CT scan of a 17-year-old girl with Parry–Romberg syndrome, showing severe loss of subcutaneous tissue and muscle of the right side of the face, with no apparent involvement of the facial bones

Initial facial changes usually involve the area of the face covered by the temporal or buccinator muscles. The disease progressively spreads from the initial location, resulting in atrophy of the skin and its adnexa, as well as underlying subcutaneous structures such as connective tissue, (fat, fascia, cartilage, bones) and/or muscles of one side of the face.[4] The mouth and nose are typically deviated towards the affected side of the face.[5]

The process may eventually extend to involve tissues between the nose and the upper corner of the lip, the upper jaw, the angle of the mouth, the area around the eye and brow, the ear, and/or the neck.[4][5] The syndrome often begins with a circumscribed patch of scleroderma in the frontal region of the scalp which is associated with a loss of hair and the appearance of a depressed linear scar extending down through the midface on the affected side. This scar is referred to as a "coup de sabre" lesion because it resembles the scar of a wound made by a sabre, and is indistinguishable from the scar observed in frontal linear scleroderma.[6][7]

In 20% of cases, the hair and skin overlying affected areas may become hyperpigmented or hypopigmented with patches of unpigmented skin. In up to 20% of cases the disease may involve the ipsilateral (on the same side) or contralateral (on the opposite side) neck, trunk, arm, or leg.[8] The cartilage of the nose, ear and larynx can be involved. The disease has been reported to affect both sides of the face in 5 to 10% of cases.[6]

Symptoms and physical findings usually become apparent during the first or early during the second decade of life. The average age of onset is nine years of age,[4] and the majority of individuals experience symptoms before 20 years of age. The disease may progress for several years before eventually going into remission (abruptly ceasing).[4]

### Neurological

Neurological abnormalities are common. Roughly 45% of people with Parry–Romberg syndrome also have trigeminal neuralgia (severe pain in the tissues supplied by the ipsilateral trigeminal nerve, including the forehead, eye, cheek, nose, mouth and jaw) and/or migraine (severe headaches that may be accompanied by visual abnormalities, nausea and vomiting).[8][9]

10% of affected individuals develop a seizure disorder as part of the disease.[8] The seizures are typically Jacksonian in nature (characterized by rapid spasms of a muscle group that subsequently spread to adjacent muscles) and occur on the side contralateral to the affected side of the face.[4] Half of these cases are associated with abnormalities in both the gray and white matter of the brain—usually ipsilateral but sometimes contralateral—that are detectable on magnetic resonance imaging (MRI) scan.[8][10]

### Ocular

Recession of the eyeball within the orbit is the most common eye abnormality observed in Parry–Romberg syndrome. It is caused by a loss of subcutaneous tissue around the orbit. Other common findings include drooping of the eyelid, constriction of the pupil, redness of the conjunctiva, and decreased sweating of the affected side of the face. Collectively, these signs are referred to as Horner's syndrome. Other ocular abnormalities include ophthalmoplegia (paralysis of one or more of the extraocular muscles) and other types of strabismus, uveitis, and heterochromia of the iris.[11][12]

### Oral

The tissues of the mouth, including the tongue, gingiva, teeth and soft palate are commonly involved in Parry–Romberg syndrome.[5] 50% of affected individuals develop dental abnormalities such as delayed eruption, dental root exposure, or resorption of the dental roots on the affected side. 35% have difficulty or inability to normally open the mouth or other jaw symptoms, including temporomandibular joint dysfunction and spasm of the muscles of mastication on the affected side. 25% experience atrophy of one side of the upper lip and tongue.[8]

## Causes

The fact that some people affected with this disease have circulating antinuclear antibodies in their serum supports the theory that Parry–Romberg syndrome may be an autoimmune disease, specifically a variant of localized scleroderma.[13] Several instances have been reported where more than one member of a family has been affected, prompting speculation of an autosomal dominant inheritance pattern. However, there has also been at least one report of monozygotic twins in which only one of the twins was affected, casting doubt on this theory. Further, the National Organization for Rare Disorders has stated there is currently no evidence that Parry–Romberg syndrome is genetic or that it can be passed on to children.[14] Various other theories about the cause and pathogenesis have been suggested, including alterations in the peripheral sympathetic nervous system (perhaps as a result of trauma or infection involving the cervical plexus or the sympathetic trunk), as the literature reported it following sympathectomy, disorders in migration of cranial neural crest cells, or chronic cell-mediated inflammatory process of the blood vessels. It is likely that the disease results from different mechanisms in different people, with all of these factors potentially being involved.[4]

## Diagnosis

Diagnosis can be made solely on the basis of history and physical examination in people who present with only facial asymmetry. For those who report neurological symptoms such as migraine or seizures, MRI scan of the brain is the imaging modality of choice. A diagnostic lumbar puncture and serum test for autoantibodies may also be indicated in people who present with a seizure disorder of recent onset.[8] Oligoclonal bands and an elevated IgG index may be found in 50% of the patients.[15]

* A 3D, soft tissue reconstruction of a CT scan of a 17-year-old girl with Parry Romberg syndrome.

* CT scan 3D bone reconstruction of a 17-year-old girl with Parry Romberg syndrome.

## Management

### Medical

Medical management may involve immunosuppressive drugs such as methotrexate, corticosteroids, cyclophosphamide, and azathioprine. No randomized controlled trials have yet been conducted to evaluate such treatments, so the benefits have not been clearly established.[8]

### Surgical

Affected individuals may benefit from autologous fat transfer or fat grafts to restore a more normal contour to the face. However, greater volume defects may require microsurgical reconstructive surgery which may involve the transfer of an island parascapular fasciocutaneous flap or a free flap from the groin, rectus abdominis muscle (Transverse Rectus Abdominis Myocutaneous or "TRAM" flap) or latissimus dorsi muscle to the face. Severe deformities may require additional procedures, such as pedicled temporal fascia flaps, cartilage grafts, bone grafts, orthognathic surgery, and bone distraction.[16] The timing of surgical intervention is controversial; some surgeons prefer to wait until the disease has run its course[5] while others recommend early intervention.[17]

## Epidemiology

Parry–Romberg syndrome appears to occur randomly and for unknown reasons. Prevalence is higher in females than males, with a ratio of roughly 3:2. The condition is observed on the left side of the face about as often as on the right side.[18]

## History

Hemifacial atrophy of the forehead and scalp, 1897

The disease was first described in 1825 by Caleb Hillier Parry (1755–1822), in a collection of his medical writings which were published posthumously by his son Charles Henry Parry (1779–1860).[19] It was described a second time in 1846 by Moritz Heinrich Romberg (1795–1873) and Eduard Heinrich Henoch (1820–1910).[20] German neurologist Albert Eulenburg (1840–1917) was the first to use the descriptive title "progressive hemifacial atrophy" in 1871.[21][22][23]

## See also

* Hemifacial microsomia
* List of skin conditions
* Trigeminal trophic syndrome

## References

1. ↑ Parry-Romberg Syndrome. StatPearls. November 8, 2022. https://www.ncbi.nlm.nih.gov/books/NBK574506/.
2. ↑ "Case 178: Parry-Romberg syndrome". Radiology 262 (2): 721–5. February 2012. doi:10.1148/radiol.11092104. PMID 22282187.
3. ↑ "Late-onset progressive facial hemiatrophy (Parry-Romberg syndrome)". J Postgrad Med 51 (2): 135–6. 2005. PMID 16006711.
4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 Gorlin, RJ; Cohen, MM; Hennekam, RCM (2001). "Chapter 24: Syndromes with unusual facies: well-known syndromes". Syndromes of the head and neck (4th ed.). New York: Oxford University Press. pp. 977–1038. ISBN 978-0-19-511861-2. https://books.google.com/books?id=mSUnOoCvQWAC&q="Parry–Romberg+syndrome22&pg=PA1020.
5. ↑ 5.0 5.1 5.2 5.3 Saraf, S (2006). "Chapter 3: Developmental disorders of oral and paraoral structures". Textbook of oral pathology. New Delhi: Jaypee Brothers Medical Publishers Ltd. pp. 31–76. ISBN 978-81-8061-655-6. https://books.google.com/books?id=WnZ0Ek2nP4wC&q=Parry&pg=PA548.
6. ↑ 6.0 6.1 Saraf, S (2006). "Features of syndromes and conditions affecting oral and extra oral structures". Textbook of oral pathology. New Delhi: Jaypee Brothers Medical Publishers Ltd. pp. 547–54. ISBN 978-81-8061-655-6. https://books.google.com/books?id=WnZ0Ek2nP4wC&q=Parry&pg=PA548.
7. ↑ Wartenberg, R (1945). "Progressive facial hemiatrophy (abstract)". Archives of Neurology and Psychiatry 54 (2): 75–97. doi:10.1001/archneurpsyc.1945.02300080003001.
8. ↑ 8.0 8.1 8.2 8.3 8.4 8.5 8.6 Stone, J (2006). "Neurological rarity: Parry-Romberg syndrome". Practical Neurology 6 (3): 185–8. doi:10.1136/jnnp.2006.089037. http://www.therombergsconnection.com/dr_stone_survey/Stone_Parry_Romberg_Practical_Neurology.pdf.
9. ↑ Parry-Romberg Syndrome at NINDS
10. ↑ "Progressive hemifacial atrophy with agenesis of the head of the caudate nucleus". Journal of Medical Genetics 31 (12): 969–71. December 1994. doi:10.1136/jmg.31.12.969. PMID 7891383.
11. ↑ "Ocular manifestations and treatment of hemifacial atrophy". American Journal of Ophthalmology 88 (5): 889–97. November 1979. doi:10.1016/0002-9394(79)90567-1. PMID 507167.
12. ↑ "Influence of various levels of acetate and glucose on the in vitro biosynthesis of lipids from 2-14C-acetate and U-14C-glucose by buffalo mammary gland slices". Zeitschrift für Tierphysiologie, Tierernahrung und Futtermittelkunde 42 (2): 57–64. August 1979. doi:10.1136/jnnp.37.9.997. PMID 494830.
13. ↑ "Progressive hemifacial atrophy (Parry-Romberg syndrome) report with review of genetics and nosology". American Journal of Medical Genetics 14 (2): 385–90. February 1983. doi:10.1002/ajmg.1320140220. PMID 6601461.
14. ↑ "Parry Romberg Syndrome". NORD's Rare Disease Database (National Organization for Rare Disorders). 2016. https://rarediseases.org/rare-diseases/parry-romberg-syndrome/.
15. ↑ "Neurological Manifestations in Parry-Romberg Syndrome: 2 Case Reports". Medicine 94 (28). July 2015. doi:10.1097/MD.0000000000001147. PMID 26181554.
16. ↑ "Restoration of facial contour in Romberg's disease and hemifacial microsomia: experience with 118 cases". Microsurgery 20 (4): 167–72. 2000. doi:10.1002/1098-2752(2000)20:4<167::AID-MICR4>3.0.CO;2-D. PMID 10980515.
17. ↑ University of Wisconsin Hospitals and Clinics Authority (2011-05-17). "UW health surgeon reconstructs young girl's face". News for referring physicians. Madison, Wisconsin: University of Wisconsin Hospitals and Clinics Authority. http://www.uwhealth.org/referring-physician-news/uw-health-surgeon-reconstructs-young-girls-face/31371.
18. ↑ Broadbent TR, Anderson B, ed (October 13–18, 1963). "Progressive facial hemiatrophy (Romberg's diseases): a review of 772 cases". Third International Congress of Plastic Surgery. Amsterdam: Excerpta Medica. pp. 681–9.
19. ↑ Parry, CH (1825). Parry, CH. ed. Collections from the unpublished medical writings of the late Caleb Hillier Parry, M.D., F.R.S.. 1. London: Underwoods. pp. 478–80.
20. ↑ Romberg, MH; Henoch, EH (1846). "Krankheiten des nervensystems (IV: Trophoneurosen)" (in de). Klinische ergebnisse. Berlin: Albert Förstner. pp. 75–81. https://books.google.com/books?id=MfxaAAAAQAAJ&q="Klinische+Ergebnisse"+1846&pg=PR1.
21. ↑ Eulenburg, A (1871). "Hemiatrophia facialis progressiva" (in de). Lehrbuch der functionellen nervenkrankheiten auf physiologischer basis. Berlin: Verlag von August Hirschwald. pp. 712–26. https://books.google.com/books?id=_bdAAAAAYAAJ&pg=PA712.
22. ↑ synd/1285 at Who Named It?
23. ↑ "Clinical and radiologic findings in progressive facial hemiatrophy (Parry-Romberg syndrome)". AJNR. American Journal of Neuroradiology 18 (4): 751–7. April 1997. PMID 9127045. PMC 8338508. http://www.ajnr.org/cgi/pmidlookup?view=long&pmid=9127045.

## Further reading

* "[Neuroretinitis, Parry-Romberg syndrome, and scleroderma]" (in fr). Journal Français d'Ophtalmologie 28 (8): 866–70. October 2005. doi:10.1016/S0181-5512(05)81008-3. PMID 16249769.
* "Progressive hemifacial atrophy with scleroderma and ipsilateral limb wasting (Parry-Romberg syndrome)". Journal of the Royal Society of Medicine 77 (2): 138–9. February 1984. doi:10.1177/014107688407700215. PMID 6737396.
* "Some observations on the aetiology of progressive hemifacial atrophy ("Parry-Romberg syndrome")". Journal of Neurology, Neurosurgery, and Psychiatry 56 (9): 1035–6. September 1993. doi:10.1136/jnnp.56.9.1035-a. PMID 8410030.
* "Progressive hemifacial atrophy. A natural history study". Transactions of the American Ophthalmological Society 93: 203–15; discussion 215–7. 1995. PMID 8719679.
* "Progressive Hemifacial Atrophy--case report". Medicina Oral, Patologia Oral y Cirugia Bucal 11 (2): E112-4. March 2006. PMID 16505785.
* "Progressive hemifacial atrophy: a case report". The British Journal of Ophthalmology 69 (7): 545–7. July 1985. doi:10.1136/bjo.69.7.545. PMID 4016051.

## External links

* Progressive hemifacial atrophy; Parry-Romberg syndrome at NIH's Office of Rare Diseases

Classification|

* ICD-10: G51.8
* ICD-9-CM: 349.89, 351.8
* OMIM: 141300
* MeSH: D005150
* DiseasesDB: 30151

|

External resources|

* Orphanet: 1214

* v
* t
* e

Diseases relating to the peripheral nervous system

Mononeuropathy

| Arm|

| median nerve|

* Carpal tunnel syndrome
* Ape hand deformity

|

ulnar nerve|

* Ulnar nerve entrapment
* Froment's sign
* Ulnar tunnel syndrome
* Ulnar claw

radial nerve|

* Radial neuropathy
* Wrist drop
* Cheiralgia paresthetica

long thoracic nerve|

* Winged scapula
* Backpack palsy

Leg|

| lateral cutaneous nerve of thigh|

* Meralgia paraesthetica

|

tibial nerve|

* Tarsal tunnel syndrome

plantar nerve|

* Morton's neuroma

superior gluteal nerve|

* Trendelenburg's sign

sciatic nerve|

* Piriformis syndrome

Cranial nerves|

* See Template:Cranial nerve disease

[[Medicine:PolyneuropatPolyneuropathy andPolyradiculoneuropathy]]

| HMSN|

* Charcot–Marie–Tooth disease
* Dejerine–Sottas disease
* Refsum's disease
* Hereditary spastic paraplegia
* Hereditary neuropathy with liability to pressure palsy
* Familial amyloid neuropathy

|

Autoimmune and demyelinating disease]]|

* Guillain–Barré syndrome
* Chronic inflammatory demyelinating polyneuropathy

[[Medicine:RadiculopatRadiculopathy]] and plexopathy|

* Brachial plexus injury
* Thoracic outlet syndrome
* Phantom limb

Other|

* Alcoholic polyneuropathy

Other

| General|

* Complex regional pain syndrome
* Mononeuritis multiplex
* Peripheral neuropathy
* Neuralgia
* Nerve compression syndrome

|

* v
* t
* e

Oral and maxillofacial pathology (K00–K06, K11–K14, 520–525, 527–529)

Lips

* Cheilitis
* Actinic
* Angular
* Plasma cell
* Cleft lip
* Congenital lip pit
* Eclabium
* Herpes labialis
* Macrocheilia
* Microcheilia
* Nasolabial cyst
* Sun poisoning
* Trumpeter's wart

Tongue

* Ankyloglossia
* Black hairy tongue
* Caviar tongue
* Crenated tongue
* Cunnilingus tongue
* Fissured tongue
* Foliate papillitis
* Glossitis
* Geographic tongue
* Median rhomboid glossitis
* Transient lingual papillitis
* Glossoptosis
* Hypoglossia
* Lingual thyroid
* Macroglossia
* Microglossia
* Rhabdomyoma

Palate

* Bednar's aphthae
* Cleft palate
* High-arched palate
* Palatal cysts of the newborn
* Inflammatory papillary hyperplasia
* Stomatitis nicotina
* Torus palatinus

Oral mucosa – Lining of mouth

* Amalgam tattoo
* Angina bullosa haemorrhagica
* Behçet's disease
* Bohn's nodules
* Burning mouth syndrome
* Candidiasis
* Condyloma acuminatum
* Darier's disease
* Epulis fissuratum
* Erythema multiforme
* Erythroplakia
* Fibroma
* Giant-cell
* Focal epithelial hyperplasia
* Fordyce spots
* Hairy leukoplakia
* Hand, foot and mouth disease
* Hereditary benign intraepithelial dyskeratosis
* Herpangina
* Herpes zoster
* Intraoral dental sinus
* Leukoedema
* Leukoplakia
* Lichen planus
* Linea alba
* Lupus erythematosus
* Melanocytic nevus
* Melanocytic oral lesion
* Molluscum contagiosum
* Morsicatio buccarum
* Oral cancer
* Benign: Squamous cell papilloma
* Keratoacanthoma
* Malignant: Adenosquamous carcinoma
* Basaloid squamous carcinoma
* Mucosal melanoma
* Spindle cell carcinoma
* Squamous cell carcinoma
* Verrucous carcinoma
* Oral florid papillomatosis
* Oral melanosis
* Smoker's melanosis
* Pemphigoid
* Benign mucous membrane
* Pemphigus
* Plasmoacanthoma
* Stomatitis
* Aphthous
* Denture-related
* Herpetic
* Smokeless tobacco keratosis
* Submucous fibrosis
* Ulceration
* Riga–Fede disease
* Verruca vulgaris
* Verruciform xanthoma
* White sponge nevus

Teeth (pulp, dentin, enamel)

* Amelogenesis imperfecta
* Ankylosis
* Anodontia
* Caries
* Early childhood caries
* Concrescence
* Failure of eruption of teeth
* Dens evaginatus
* Talon cusp
* Dentin dysplasia
* Dentin hypersensitivity
* Dentinogenesis imperfecta
* Dilaceration
* Discoloration
* Ectopic enamel
* Enamel hypocalcification
* Enamel hypoplasia
* Turner's hypoplasia
* Enamel pearl
* Fluorosis
* Fusion
* Gemination
* Hyperdontia
* Hypodontia
* Maxillary lateral incisor agenesis
* Impaction
* Wisdom tooth impaction
* Macrodontia
* Meth mouth
* Microdontia
* Odontogenic tumors
* Keratocystic odontogenic tumour
* Odontoma
* Dens in dente
* Open contact
* Premature eruption
* Neonatal teeth
* Pulp calcification
* Pulp stone
* Pulp canal obliteration
* Pulp necrosis
* Pulp polyp
* Pulpitis
* Regional odontodysplasia
* Resorption
* Shovel-shaped incisors
* Supernumerary root
* Taurodontism
* Trauma
* Avulsion
* Cracked tooth syndrome
* Vertical root fracture
* Occlusal
* Tooth loss
* Edentulism
* Tooth wear
* Abrasion
* Abfraction
* Acid erosion
* Attrition

Periodontium (gingiva, periodontal ligament, cementum, alveolus) – Gums and tooth-supporting structures

* Cementicle
* Cementoblastoma
* Gigantiform
* Cementoma
* Eruption cyst
* Epulis
* Pyogenic granuloma
* Congenital epulis
* Gingival enlargement
* Gingival cyst of the adult
* Gingival cyst of the newborn
* Gingivitis
* Desquamative
* Granulomatous
* Plasma cell
* Hereditary gingival fibromatosis
* Hypercementosis
* Hypocementosis
* Linear gingival erythema
* Necrotizing periodontal diseases
* Acute necrotizing ulcerative gingivitis
* Pericoronitis
* Peri-implantitis
* Periodontal abscess
* Periodontal trauma
* Periodontitis
* Aggressive
* As a manifestation of systemic disease
* Chronic
* Perio-endo lesion
* Teething

Periapical, mandibular and maxillary hard tissues – Bones of jaws

* Agnathia
* Alveolar osteitis
* Buccal exostosis
* Cherubism
* Idiopathic osteosclerosis
* Mandibular fracture
* Microgenia
* Micrognathia
* Intraosseous cysts
* Odontogenic: periapical
* Dentigerous
* Buccal bifurcation
* Lateral periodontal
* Globulomaxillary
* Calcifying odontogenic
* Glandular odontogenic
* Non-odontogenic: Nasopalatine duct
* Median mandibular
* Median palatal
* Traumatic bone
* Osteoma
* Osteomyelitis
* Osteonecrosis
* Bisphosphonate-associated
* Neuralgia-inducing cavitational osteonecrosis
* Osteoradionecrosis
* Osteoporotic bone marrow defect
* Paget's disease of bone
* Periapical abscess
* Phoenix abscess
* Periapical periodontitis
* Stafne defect
* Torus mandibularis

Temporomandibular joints, muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities

* Bruxism
* Condylar resorption
* Mandibular dislocation
* Malocclusion
* Crossbite
* Open bite
* Overbite
* Overeruption
* Overjet
* Prognathia
* Retrognathia
* Scissor bite
* Maxillary hypoplasia
* Temporomandibular joint dysfunction

Salivary glands

* Benign lymphoepithelial lesion
* Ectopic salivary gland tissue
* Frey's syndrome
* HIV salivary gland disease
* Necrotizing sialometaplasia
* Mucocele
* Ranula
* Pneumoparotitis
* Salivary duct stricture
* Salivary gland aplasia
* Salivary gland atresia
* Salivary gland diverticulum
* Salivary gland fistula
* Salivary gland hyperplasia
* Salivary gland hypoplasia
* Salivary gland neoplasms
* Benign: Basal cell adenoma
* Canalicular adenoma
* Ductal papilloma
* Monomorphic adenoma
* Myoepithelioma
* Oncocytoma
* Papillary cystadenoma lymphomatosum
* Pleomorphic adenoma
* Sebaceous adenoma
* Malignant: Acinic cell carcinoma
* Adenocarcinoma
* Adenoid cystic carcinoma
* Carcinoma ex pleomorphic adenoma
* Lymphoma
* Mucoepidermoid carcinoma
* Sclerosing polycystic adenosis
* Sialadenitis
* Parotitis
* Chronic sclerosing sialadenitis
* Sialectasis
* Sialocele
* Sialodochitis
* Sialosis
* Sialolithiasis
* Sjögren's syndrome

Orofacial soft tissues – Soft tissues around the mouth

* Actinomycosis
* Angioedema
* Basal cell carcinoma
* Cutaneous sinus of dental origin
* Cystic hygroma
* Gnathophyma
* Ludwig's angina
* Macrostomia
* Melkersson–Rosenthal syndrome
* Microstomia
* Noma
* Oral Crohn's disease
* Orofacial granulomatosis
* Perioral dermatitis
* Pyostomatitis vegetans

Other

* Eagle syndrome
* Hemifacial hypertrophy
* Facial hemiatrophy
* Oral manifestations of systemic disease

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Parry–Romberg syndrome. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Medicine:Parry–Romberg_syndrome&oldid=4169068"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template