icd 10 code for graham little syndrome

Full Answer

What is Graham Little syndrome and what causes it?

Graham Little syndrome is a rare variant of lichen planopilaris, an inflammatory form of scarring hair loss. It is also known as Graham Little-Piccardi-Lassueuer syndrome, in various combinations and permutations of these three names. Who gets Graham Little syndrome and why?

What is the ICD 10 code for predominate malform syndromes?

Q87.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Congenital malform syndromes predom assoc w short stature. The 2018/2019 edition of ICD-10-CM Q87.1 became effective on October 1, 2018.

What is the ICD 10 code for syndromes with short stature?

Q87.19 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Other congen malform synd predom assoc with short stature The 2021 edition of ICD-10-CM Q87.19 became effective on October 1, 2020.

What is the latest version of ICD 10 for Biedl syndrome?

The 2021 edition of ICD-10-CM Q87.89 became effective on October 1, 2020. This is the American ICD-10-CM version of Q87.89 - other international versions of ICD-10 Q87.89 may differ. Applicable To. Laurence-Moon (-Bardet)-Biedl syndrome. The following code (s) above Q87.89 contain annotation back-references.

What is Graham Little syndrome?

Graham Little-Piccardi-Lassueur syndrome is a type of lichen planopilaris (follicular lichen planus) characterized by the triad of patchy cicatricial alopecia of the scalp, noncicatricial alopecia of the axilla and groin, and a follicular spinous papule on the body, scalp, or both.

What is piccardi?

Abstract. Graham–Little–Piccardi syndrome (GLPS) is a rare form of follicular lichen planus and comprises cicatricial alopecia of the scalp, noncicatricial alopecia of the axillae, and/or pubis and spinous follicular papules involving the trunk and extremities.

What causes frontal fibrosing alopecia?

The cause of FFA is unknown. It is thought that hormones may be partially responsible, as it typically affects post-menopausal women and can occur alongside genetic hair loss (also known as androgenetic or female pattern hair loss). However, blood tests for hormone levels don't usually show any abnormalities.

What is scarring hairloss?

Scarring, or cicatricial alopecia, is an inflammatory condition that destroys hair follicles, causing scarring and permanent hair loss. The Mount Sinai's Alopecia Center of Excellence can help. Dermatologists have deep experience diagnosing and treating this form of alopecia.

How is Graham Little syndrome diagnosed?

Graham Little syndrome is suspected clinically when the three features are present.

Who gets Graham Little syndrome and why?

Graham Little syndrome most commonly affects women in the age range 30-70 years, and in particular the middle-aged post-menopausal group.

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When will the ICD-10-CM Q87.2 be released?

The 2022 edition of ICD-10-CM Q87.2 became effective on October 1, 2021.

What is the genetic mutation of the lmx1b gene?

A rare autosomal dominant syndrome caused by mutations in the lmx1b gene. It is characterized by fingernail deformities, absence or hypoplasia of the patellae, iliac horns, deformities of the radial heads, nephropathy, and glaucoma. A rare genetic syndrome mapped to chromosome 16p13.3 and associated with mutations in the crebbp gene.

Is Klippel-Trenaunay-Weber syndrome normal?

Most patients have normal mentality, except when vascular lesions invade the cerebral tissue. In the absence of arteriovenous fistulae, the syndrome is often referred to as weber syndrome or parkes weber syndrome. Klippel-trenaunay-weber syndrome is associated in some cases with sturge-weber angiomatosis.

When will the ICD-10-CM Q87.1 be released?

The 2022 edition of ICD-10-CM Q87.1 became effective on October 1, 2021.

What is the phenotype of noonan syndrome?

Noonan syndrome occurs in both males and females with a normal karyotype (46,xx and 46,xy). Mutations in a several genes (ptpn11, kras, sos1, nf1 and raf1) have been associated the the ns phenotype. Mutations in ptpn11 are the most common.

What is the clinical description of turner syndrome?

Clinical Information. A cardiofacial syndrome with a variable phenotype, which may change with age, many characteristics of which overlap those of the turner syndrome. Short stature and mild mental retardation are the main features of this syndrome.

What is the phenotype of dwarfism?

The phenotype varies from normal growth and head circumference with mild psychomotor retardation and lack of eczema to severe growth and mental retardation, microcephaly, behavioral problems, aplastic anemia, immunological disorders, neoplasms, and eczema some features of this syndrome are similar to those in bloom and fetal alcohol syndromes.

What is a rare disorder characterized by low birth weight, delayed growth, mental retardation, behavioral problems, and?

The majority of cases are caused by mutations in the nipbl gene. Less severe forms of the syndrome are caused by mutations in the smc1a and smc3 genes.

What is the overlap between Leopard syndrome and Neurofibromatosis?

In addition, there is overlap with the syndrome called neurofibromatosis-noonan syndrome due to mutations in nf1. A rare autosomal recessive or dominant inherited disorder.

What is autosomal recessive disorder?

A rare autosomal recessive or dominant inherited disorder. The autosomal recessive form is caused by mutations in the ror2 gene. There is no causative mutation identified for the autosomal dominant form. It is manifested with short limbs, abnormal facial features, underdeveloped genitalia, and wedge-shaped vertebrae.